Quick answers
- What is Camphor, (-)- used for?
- The Drug Facts label of Plantar Fasciitis Cream (Solalia LLC) lists these uses: - helps relieve minor foot and heel discomfort such as: arch tightness, stiffness, soreness linked to plantar fasciitis, ired or overused feet.
- Do I need a prescription for Camphor, (-)-?
- 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 ingredient, 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, (-)- 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.
Plantar Fasciitis Cream · Solalia LLC
Camphor, (-)- 50 mg/mL, cream (topical)
Active ingredient
Camphor 5%
Purpose
Topical Analgesic
Uses
- helps relieve minor foot and heel discomfort such as: arch tightness, stiffness, soreness linked to plantar fasciitis, ired or overused feet
Warnings
For external use, do not take orally or get into eyes
Do not use
on open wounds. if there are abnormalities such as skin rashes and allergies, do not scratch. Avoid contact with eyes and mucous membranes If you experience an allergic reaction, discontinue use and consult a physician If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Clean the affected area before use. Take an appropriate amount of this product and apply it evenly on the affected area, massage until completely absorbed. Adults and children 12+, apply to affected area up to 3-4 times daily. Children under 12, ask a doctor.
Other information
Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).
Inactive ingredients
Water, Glycerin, Angelica Sinensis Root, Taraxacum Officinale, Safflower, Black Pepper, Clove, Cinnamon, Cinnamomum Cassia Twig, Ligusticum Wallichii Root, Wormwood, Stearic Acid, Glyceryl Monostearate, Methylparaben, Phenoxyethanol, Borneol
Questions?
please contact us at: scogurei@gmail.com
— FDA label of Plantar Fasciitis Cream, Solalia LLC, effective June 27, 2025. See the official label on DailyMed →
Vicks Vaposteam Lavender · Kaz USA, Inc
Camphor, (-)- 0.062 g/mL, inhalant (respiratory (inhalation))
Active ingredient
Camphor (Synthetic) 6.2%
Purpose
Cough suppressant
Uses
temporarily relieves cough associated with a cold temporarily helps you cough less. cough suppressant which temporarily controls the impulse to cough. temporarily helps to suppress the cough reflex that causes coughing. temporarily reduces the intensity of coughing. reduces your cough to help you rest.
Warnings
For external use only. Flammable Keep away from fire or flame. For steam inhalation only. DO NOT TAKE BY MOUTH.
Ask a doctor before use if
you have a persistent or chronic cough such as occurs with smoking, asthma or emphysema. cough that occurs with too much phlegm (mucus).
When using this product
do not heat microwave use near an open flame direct steam from the vaporizer or humidifier too close to the face. add to hot water or any container where heating water except when adding to cold water in a hot steam vaporizer. May cause splattering and result in burns.
Stop use and ask a doctor if
cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash or persistent headache. A persistent cough may be a sign of a serious condition.
If pregnant or breast-feeding
ask a health professional before use.
Keep out of reach of children
In case of eye exposure flush eyes with water; or if swallowed, get medical help or contact a Poison Control Center right away.
Directions
see important warnings under " When using this product ". adults & children 2 years & over: add 1 tablespoonful of solution to each quart of water OR 1½ teaspoonfuls of solution to each pint of water OR add 0.5 fl oz (1 tablespoonful) of VapoSteam liquid to medicine cup found on Warm Mist and Cool Mist Humidifiers that accept VapoSteam. follow manufacturer's directions for using vaporizer. add solution directly to cold water only in a hot steam vaporizer. breathe in the medicated vapors. use up to three times daily or as directed by a doctor. children under 2 years: do not use.
Inactive ingredients
Alcohol, Cedar Leaf Oil, Silicone, Eucalyptus Oil, Laureth-7, Lavender Oil, Menthol, Nutmeg Oil, Poloxamer 124
Questions?
1-800-VAPOR-1-2 (1-800-827-6712) Monday – Friday 8am to 6pm EST.
— FDA label of Vicks Vaposteam Lavender, Kaz USA, Inc, effective December 19, 2024. 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 ingredient, 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, (-)- 50 mg/mL · cream (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Plantar Fasciitis Cream | Solalia LLC | DailyMed |
Camphor, (-)- 0.062 g/mL · inhalant (respiratory (inhalation)) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Vicks Vaposteam Lavender | Kaz USA, 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.
- Solalia LLC1 product
- Kaz USA, Inc1 product
Recalls
No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.
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.