Quick answers
- What is Camphor (synthetic), capsaicin and menthol used for?
- The Drug Facts label of Pain Relieving (Ahc Ventures Corp DBA Cry) lists these uses: Temporary relieves minor aches and pains associated with sore muscles and joints arthritis backache muscle strains sprains bruises.
- Do I need a prescription for Camphor (synthetic), capsaicin and menthol?
- 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 (synthetic), capsaicin and menthol 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.
Pain Relieving · Ahc Ventures Corp DBA Cry
Camphor (synthetic) 3.85% · Capsaicin 0.0355% · Menthol 3.85%, lotion (topical)
Active ingredient
Menthol USP 3.85% Camphor USP 3.85% Capsaicin USP 0.0355%
Purpose
Pain Reliever
Uses
Temporary relieves minor aches and pains associated with sore muscles and joints arthritis backache muscle strains sprains bruises
Warnings
For external use only
When using this product
Use only as directed. Do not bandage or use a heating pad or device. Avoid contact with eyes and mucous membranes. Do not apply to open wounds or damaged skin.
Do not use
with other ointment, creams, sprays or liniments. After applying wash hands thoroughly with cool water
Stop use and ask a doctor if
Condition worsens or symptoms persist for more than 7 days or clear up and recur. Redness is present or irritatio develops If pregnant or Breast Feeding: Ask a health professional before use Keep Out of Reach of Children In case of accidental ingestion get medical help or contact a Poison Control Center immediately
Other information
Store in a cool dry place with lid or cap closed tightly.
- Flammable: Keep away from excessive heat or open flame
Inactive ingredients
Aloe Vera, Arnica Extract, Boswellia Serrata Extract, Green Tea Extract, Carbomer, Cetearyl Alcohol, Cetearyl Glucoside, Orange Fruit Extract, Grapefruit Extract, Dimethyl Sulfone, Ethylhexylglycerin, Glycerin, Ilex Paraguariensis Leaf Extract, Phenoxyethanol, Purified Water, Rose Extract, Vitamin E, Triethanolamine, Yucca Extract
— FDA label of Pain Relieving, Ahc Ventures Corp DBA Cry, effective September 2, 2025. See the official label on DailyMed →
Pain Relief Roll On · Eagle Labs Inc
Camphor (synthetic) 5% · Capsaicin 0.025% · Menthol 6%, liquid (topical)
Active ingredient
Menthol 6% Camphor 5% Capsaicin 0.025%
Purpose
Topical Analgesic
Uses
For the temporary relief of aches and pains of muscles and joints associated with arthritis, backaches, strains or sprains
Warnings
For External use only
When using this product
Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply directly to wounds or damaged skin.
Do not use
in combination with other ointments, creams, or sprays. Wash hand with cool water after each uyse.
Do not use
with a heating pad or device. Stop usage immediately and ask a doctor if: Condition worsens or symptoms persist for more than 7 days
If pregnant or breast-feeding
Ask a health professional before use
Keep out of reach of children
: If ingested get medical help or contact Poison control center immediately: 1-800-222-1222
Directions
Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor
Inactive ingredients
Citrus Fiber, Dimethicone, Isopropyl Alcohol, Jojoba Oil, Phenoxyethanol, Simethicone, Water
— FDA label of Pain Relief Roll On, Eagle Labs Inc, effective January 14, 2026. See the official label on DailyMed →
External Analgesic · Hmong 21
Camphor (synthetic) 9.6% · Capsaicin 0.05% · Menthol 7.8%, patch (topical)
Active ingredient
Camphor 9.6% Capsaicin 0.05% Menthol 7.8%
Purpose
External Analgesic
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with -simple backache -arthritis -strains -bruises -sprains
Warnings
When using this product
-avoid contact with the eyes - do not apply to wounds or damaged skin -do not bandage tightly
Stop use and ask a doctor if
- condition worsens -if synthoms oersust 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 12 years of age and older: -Clean and dry affected area. -Remove from backing film and apply. -Remove from the skin after at most 8 hours' application. -Apply to the affected area not more than 3 times daily. -Children under 12 years of age: Consult a doctor.
Inactive ingredients
Acrylic Acid, Aluminum Hydroxide, Carmellose Sodium, 2-ethylhexylacrylate, Glycerin, Methyl Acrylate, Polyacrylate, polyacrylic Acid, sodium polyacrylatem, Tartaric Acid, Water.
— FDA label of External Analgesic, Hmong 21, effective December 26, 2023. 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 (synthetic) 3.85% · Capsaicin 0.0355% · Menthol 3.85% · lotion (topical) · 2 products
Camphor (synthetic) 4% · Capsaicin 0.025% · Menthol 3% · cream (transdermal) · 1 product
| Brand or product name | Company on the label | Label |
|---|---|---|
| Jelvoxa Dmso | Vange Life Technology Co., Limited | — |
Camphor (synthetic) 11% · Capsaicin 0.1% · Menthol 16% · spray (topical) · 1 product
| Brand or product name | Company on the label | Label |
|---|---|---|
| Pain Relief | Fullstack Fulfillment | — |
Camphor (synthetic) 5% · Capsaicin 0.025% · Menthol 6% · liquid (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Pain Relief Roll On | Eagle Labs Inc | DailyMed |
Camphor (synthetic) 9.6% · Capsaicin 0.05% · Menthol 7.8% · patch (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| External Analgesic | Hmong 21 | 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.
- Ahc Ventures Corp DBA Cry2 products
- Vange Life Technology Co., Limited1 product
- Fullstack Fulfillment1 product
- Eagle Labs Inc1 product
- Hmong 211 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
- 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.