Quick answers
- What is Camphor (natural) and phenol used for?
- The Drug Facts label of DDM Instant Antiseptic Pain Relief (Discount Drug Mart) lists these uses: Helps prevent infection and temporarily relieves pain and itching in minor burns, cuts, insect bites, scrapes, sunburn and other minor skin irritations..
- Do I need a prescription for Camphor (natural) and phenol?
- 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 phenol 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.
DDM Instant Antiseptic Pain Relief · Discount Drug Mart
Camphor (natural) 108 mg/mL · Phenol 47 mg/mL, liquid (topical)
Active ingredient
Camphor 10.8%, Phenol 4.7 %
Purpose
Pain Reliever, Antiseptic
Uses
Helps prevent infection and temporarily relieves pain and itching in minor burns, cuts, insect bites, scrapes, sunburn and other minor skin irritations.
Warnings
For External Use Only. Do not induce vomiting. If vomiting occurs give fluids again.
Do not use
in or near the eyes: In case of eye contact, flush eyes with running water for 15 minutes, get medical attention immediately.
Do not use
on: deep punture wounds, animal bites, serious burns.
When using this product
Do not bandage.
Do not use
over large areas of the body. Stop use and consult a doctor if: Condition worsens. Symptoms last more than 7 days or clear up and occur again in a few days. Keep out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions
Adult and children 2 yrs and older: apply to affected area 1 to 3 times daily. Children under 2 yrs of age: Consult a doctor before use.
Inactive ingredients
Citric acid, Eucalyptus Oil, Light Mineral Oil
— FDA label of DDM Instant Antiseptic Pain Relief, Discount Drug Mart, effective December 19, 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 (natural) 108 mg/mL · Phenol 47 mg/mL · liquid (topical) · 5 products
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| Antiseptic Instant Pain Relief | Pharma Nobis, LLC | DailyMed |
| DDM Instant Antiseptic Pain Relief | Discount Drug Mart | DailyMed |
| HEB Camphor Phenol | H E B | DailyMed |
| Instant Antiseptic Pain Relief | Chain Drug Market Association | DailyMed |
| Premier Value Instant Antiseptic Pain Relief | Pharmacy Value Alliance LLC | 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.
- Pharmacy Value Alliance LLC1 product
- H E B1 product
- Chain Drug Market Association1 product
- Discount Drug Mart1 product
- Pharma Nobis, LLC1 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.