Quick answers
- What is Allantoin and lidocaine used for?
- The Drug Facts label of OKeeffes Healthy Feet (The Gorilla Glue Company/O'Keeffe's Company) lists these uses: temporarily relieves pain and itching associated with minor skin irritations protects and helps relieve chapped or cracked skin.
- Do I need a prescription for Allantoin and lidocaine?
- 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 Allantoin and lidocaine 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.
OKeeffes Healthy Feet · The Gorilla Glue Company/O'Keeffe's Company
Allantoin 0.5% · Lidocaine hydrochloride 4%, cream (topical)
Active ingredient
Allantoin 0.5% Lidodaine HCl 4%
Purpose
Skin protectant Topical analgesic
Uses
temporarily relieves pain and itching associated with minor skin irritations protects and helps relieve chapped or cracked skin
Warnings
For external use only
Do not use
in large quantities, particularly over raw surfaces or blistered areas. on deep or puncture wounds, animal bites or serious burns
When using this product
avoid contact with eyes
Stop use and ask a doctor if
condition worsens symptoms last 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: Apply to affected area not more than 3 to 4 times daily. children under 12 years of age: consult a doctor.
Inactive ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aluminum Starch Octenylsuccinate, Beeswax, Caprylyl Glycol, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, 1,2 Hexanediol, Isopropyl Myristate, Laureth-12, PEG-100 Stearate, Peppermint (Mentha Piperita) Oil, Phenoxyethanol, Polysilicone-11, Shea (Butyrospermum Parkii) Butter, Sodium Hydroxide, Water, Xanthan Gum
Questions?
1-800-275-2718
— FDA label of OKeeffes Healthy Feet, The Gorilla Glue Company/O'Keeffe's Company, effective January 1, 2024. See the official label on DailyMed →
DermaRad Relief · Renu Laboratories, LLC
Allantoin 1.18 g/118 mL · Lidocaine 4.72 g/118 mL, emulsion (topical)
Active ingredient
Allantoin 1% Lidocaine 4%
Purpose
Skin Protectant Topical Analgesic
Uses
For the temporary relief of pain and itching associated with minor burns, sunburn, or minor skin irritations. Temporarily protects minor burns. Temporarily protects and helps relieve chapped or cracked skin.
Warnings
For External Use Only Avoid contact with the eyes. If condition worsens or if symptoms last more than 7 days or clear up and occur again within a few days, discontinue use and consult a physician.
Do not use
on: Deep or puncture wounds Animal bites Serious burns
Do not use
in large quantities, particularly over raw surfaces or blistered areas.
Do not use
on: Deep or puncture wounds Animal bites Serious burns
Do not use
in large quantities, particularly over raw surfaces or blistered areas.
Keep out of reach of children
Directions
Adults and children 2 years of age and older, apply to affected areas no more than 3 to 4 times daily. For children under 2 years of age, consult your physician.
Inactive ingredients
Capric/Caprylic Triglyceride, Capryl Glycol, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Deionized Water, Dihydroeugenol, Dimethicone, Dimethyl Isosorbide, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Glycol Stearate, Hexylene Glycol, Hydroxypropyl Starch Phosphate, Isoeugenyl Acetate, Niacinamide, PEG-100 Stearate, Petrolatum, Phenoxyethanol, Polyacrylate Crosspolymer-6, PPG/SMDI Copolymer, Propylene Glycol, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium PCA, Squalane, Stearic Acid, Tocopherol.
Questions?
DermaMedics LLC, Oklahoma City, OK 73104 www.dermamedics.com 1-800-990-6552
— FDA label of DermaRad Relief, Renu Laboratories, LLC, effective May 6, 2025. 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.
Allantoin 0.5% · Lidocaine hydrochloride 4% · cream (topical) · 2 products
Allantoin 1.18 g/118 mL · Lidocaine 4.72 g/118 mL · emulsion (topical) · 1 product
Drug Facts for this strength and form ↑
| Brand or product name | Company on the label | Label |
|---|---|---|
| DermaRad Relief | Renu Laboratories, 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.
- The Gorilla Glue Company/O'Keeffe's Company2 products
- Renu Laboratories, 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.