Quick answers
- What is Camphor (natural) and menthol, unspecified form used for?
- The Drug Facts label of Eternal Spirit Beauty Painless Pain Relieving (Worldwide Cosmetics, Inc) lists these uses: For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.
- Do I need a prescription for Camphor (natural) and menthol, unspecified form?
- No. The products on this page are sold without a prescription (over the counter).
- Is a store brand the same as the name brand?
- Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
- Has Camphor (natural) and menthol, unspecified form been recalled?
- No recall linked to these products appears in the FDA enforcement reports we use.
Drug Facts label
Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.
Eternal Spirit Beauty Painless Pain Relieving · Worldwide Cosmetics, Inc
Camphor (natural) 3% · Menthol, unspecified form 10%, cream (topical)
Active ingredient
Menthol 10% Camphor 3%
Purpose
External Analgesic Pain Relieving
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains
Warnings
- Use only as directed.
- For external use only.
- Do not bandage tightly.
Do not use
with heating pad, pack, wrap, hot water bottle or any heating element. If swallowed, get medical help, or contact a Poison Control Center right away.
Directions
- Adults and children over 2 years of age; apply a thin layer to the affected area and rub gently not more than 3 to 4 times daily.
- Wash hands with soap and water after use.
- Children under 2 years of age; do not use unless directed by doctor.
Inactive ingredients
Aqua, Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Glyceryl Stearate, Dimethicone, Glycereth-26, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Parfum, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Linalool, Limonene, Benzyl Benzoate, Coumarin.
— FDA label of Eternal Spirit Beauty Painless Pain Relieving, Worldwide Cosmetics, Inc, effective August 21, 2026. See the official label on DailyMed →
Pain Relieving Liniment · J.R. Watkins, LLC.
Camphor (natural) 3.5% · Menthol, unspecified form 2.5%, spray (topical)
Active ingredient
Purpose CAMPHOR 3.5% EXTERNAL ANALGESIC MENTHOL 2.5% EXTERNAL ANALGESIC
Purpose
Active ingredients Purpose CAMPHOR 3.5% EXTERNAL ANALGESIC MENTHOL 2.5% EXTERNAL ANALGESIC
Uses
Provides penetrating pain relief temporarily relieves minor aches and pains of muscles and joints associated with simple backache strains bruises sprains arthritis
Warnings
For external use only
- Flammable: Keep away from fire or flame.
When using this product
avoid contact with eyes, nostrils and mouth do not bandage tightly do not apply to wounds or damaged skin
Stop use and ask a doctor if
condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days rash or irritation occurs
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Adults and children 2 years and older: Apply to affected area not more than 3-4 times daily. Children under 2 years of age: Ask a doctor.
Inactive ingredients
Eucalyptus globulus leaf oil, polysorbate 20, SD Alcohol 40B, thymol, water.
Questions?
1-800-243-9423
— FDA label of Pain Relieving Liniment, J.R. Watkins, LLC., effective April 2, 2024. See the official label on DailyMed →
Menthol Camphor Cough Suppressant Topical Analgesic Rub · J.R. Watkins, LLC.
Camphor (natural) 5.3% · Menthol, unspecified form 2.8%, ointment (topical)
Active ingredient
Purpose CAMPHOR 5.3% Cough Suppressant/topical analgesic MENTHOL 2.8% Cough Suppressant/topical analgesic
Purpose
Active Ingredients Purpose CAMPHOR 5.3% Cough Suppressant/topical analgesic MENTHOL 2.8% Cough Suppressant/topical analgesic
Uses
temporarily relieves cough due to a cold minor aches and pains of muscles and joint
Warnings
For external use only. Avoid contact with eyes.
Do not use
by mouth in nostrils on wounds or damaged skin with a tight bandage
Ask a doctor before use if
you have cough that occurs with too much phlegm (mucus) chronic cough that lasts such as occurs with smoking, asthma, or emphysema
When using this product
do not heat microwave add to hot water or any container where heating water. May cause splattering and result in burns.
Stop use and ask a doctor if
muscle aches and pains last more than 7 days or clear up and occur again within a few days cough last more than 7 days, comes back or occurs with fever, rash, or persistent headache. These could be signs of a serious condition.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
see important warnings under 'When using this product' Adults and children 2 years and older: For cough rub on the throat and chest in a thick layer cover with a warm, dry cloth if desired clothing should be loose about throat and chest to help vapors reach the nose and mouth use up to three times daily or as directed by a doctor For muscle aches and pain apply to affected area not more than 3 to 4 times daily children under 2 years of age: do not use
Inactive ingredients
paraffin, petrolatum
Questions?
1-888-384-1945
— FDA label of Menthol Camphor Cough Suppressant Topical Analgesic Rub, J.R. Watkins, LLC., effective February 8, 2024. See the official label on DailyMed →
Earths Care Anti-Itch · DLC Laboratories, Inc.
Camphor (natural) 0.5% · Menthol, unspecified form 1%, lotion (topical)
Active ingredient
Camphor 0.5% external analgesic Menthol 1% external analgesic Active ingredients Purpose Camphor 0.5% External analgesic Menthol 1% External analgesic
Purpose
Active ingredients Purpose Camphor 0.5% External analgesic Menthol 1% External analgesic
Uses
for the temporary relief of pain and itching associated with minor skin irritations such as poison ivy/oak/sumac, sunburn, insect bites, and minor cuts and scrapes.
Warnings
For external use only
When using this product
avoid contact with eyes
Stop use and ask a doctor if
condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days
If pregnant or breast-feeding
ask a health professional before use.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
When using this product
avoid contact with eyes
When using this product
avoid contact with eyes
Directions
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.
Inactive ingredients
Aloe barbadensis (aloe vera ) leaf juice powder, alpha-bisabolol, Argania spinosa (argan) kernel oil, benzyl alcohol, Butyrospermum parkii (shea) butter, caprylic/capric triglyceride, cetyl alcohol, cetyl hydroxyethylcellulose, ethylhexylglycerin, glycerin, glyceryl stearate, heptyl undecylenate, Persea gratissima (avocado) oil, phenoxyethanol, polyglyceryl-3 dicitrate/stearate, potassium hydroxide, Prunus amygdalus dulcis (sweet almond) oil, purified water, Simmondsia chinensis (jojoba) seed oil, tocopherol (natural vitamin E), Zingiber officinale (ginger) root extract.
Questions?
1-888-602-6380 earths-care.com Distributed by Earth's Care Natural Products, Inc. Long Beach, California 90805, USA
— FDA label of Earths Care Anti-Itch, DLC Laboratories, Inc., effective June 13, 2025. See the official label on DailyMed →
Mentholatum Original · The Mentholatum Company
Camphor (natural) 9% · Menthol, unspecified form 1.3%, ointment (topical)
Active ingredient
Camphor 9% Menthol 1.3%
Purpose
Camphor - Topical Analgesic Menthol - Topical Analgesic
Uses
temporarily relieves minor aches and pains of muscles and joints
Warnings
For external use only
When using this product
do not get into eyes do not apply to wounds or to damaged skin do not bandage tightly do not heat, microwave, or add to hot water as this may cause splattering and result in burns
Stop use and ask a doctor if
condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily children under 2 years: ask a doctor
Inactive ingredients
fragrance, petrolatum, titanium dioxide
Questions?
1-877-636-2677 MON-FRI 9AM to 5PM (EST)
— FDA label of Mentholatum Original, The Mentholatum Company, effective December 13, 2024. See the official label on DailyMed →
Earths Care Anti-Itch · DLC Laboratories, Inc.
Camphor (natural) 0.5% · Menthol, unspecified form 1%, cream (topical)
Active ingredient
Purpose Camphor 0.5% External analgesic Menthol 1% External analgesic
Purpose
Active ingredients Purpose Camphor 0.5% External analgesic Menthol 1% External analgesic
Uses
for the temporary relief of pain and itching associated with minor skin irritations such as poison ivy/oak/sumac, sunburn, insect bites, and minor cuts and scrapes
Warnings
For external use only
When using this product
avoid contact with the eyes
Stop use and ask a doctor if
condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days
If pregnant or breast-feeding
ask a health professional before use.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.
Inactive ingredients
beeswax, Butyrospermum parkii (shea) butter, cetearyl glucoside, cetyl alcohol, citric acid, glycerin, glyceryl stearate, heptyl undecylenate, hydrogenated castor oil, Oryza sativa (rice) bran extract, phenoxyethanol, potassium sorbate, Prunus amygdalus dulcis (sweet almond) oil, purified water, sodium stearoyl glutamate, sodium stearoyl lactylate, stearic acid, xanthan gum
— FDA label of Earths Care Anti-Itch, DLC Laboratories, Inc., effective January 13, 2026. See the official label on DailyMed →
This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.
Same medicine, other brands
Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.
Camphor (natural) 3% · Menthol, unspecified form 10% · cream (topical) · 10 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Eternal Spirit Beauty Pain Relief with Hemp | Worldwide Cosmetics, Inc | DailyMed |
| Eternal Spirit Beauty Painless Pain Relieving | Worldwide Cosmetics, Inc | DailyMed |
| Menthol, Camphor | Chemco Corporation | DailyMed |
| Menthol, Camphor | Sunset Novelties, Inc | DailyMed |
| Menthol, Camphor | Sunset Pain Relief | DailyMed |
| Menthol, Camphor | Sunset Potent Pain Relief | DailyMed |
Camphor (natural) 3.5% · Menthol, unspecified form 2.5% · spray (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Pain Relieving Liniment | J.R. Watkins, LLC. | DailyMed |
Camphor (natural) 5.3% · Menthol, unspecified form 2.8% · ointment (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Menthol Camphor Cough Suppressant Topical Analgesic Rub | J.R. Watkins, LLC. | DailyMed |
Camphor (natural) 0.5% · Menthol, unspecified form 1% · lotion (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Earths Care Anti-Itch | DLC Laboratories, Inc. | DailyMed |
Camphor (natural) 9% · Menthol, unspecified form 1.3% · ointment (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Mentholatum Original | The Mentholatum Company | DailyMed |
Camphor (natural) 0.5% · Menthol, unspecified form 1% · cream (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Earths Care Anti-Itch | DLC Laboratories, Inc. | DailyMed |
Companies that sell this medicine
The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.
- Chemco Corporation3 products
- Sunset Pain Relief3 products
- J.R. Watkins, LLC.2 products
- Worldwide Cosmetics, Inc2 products
- DLC Laboratories, Inc.2 products
- The Mentholatum Company1 product
- Sunset Potent Pain Relief1 product
- Sunset Novelties, Inc1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youA pharmacist can answer questions about this label
- Earths CareBrand page: products, maker and price
- Latest FDA drug recallsPrescription and over-the-counter, newest first
- All over-the-counter medicinesSearch by ingredient, brand or Spanish name
Sources
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- FDA rule for the Drug Facts label (21 CFR 201.66)
Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.