DerMend Moisturizing Anti-Itch
Pramoxine hydrochloride · Lotion · Topical
Active ingredient
Active ingredient Pramoxine HCl 1% w/w
Purpose
Purpose external analgesic
Uses
Use for the temporary relief of itching associated with minor skin irritations
Warnings
Warnings For external use only. Avoid contact with the eyes. Stop use and ask a doctor if conditions worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Cotrol Center right away.
Stop use and ask a doctor
Stop use and ask a doctor if conditions worsens symptoms last more than 7 days or clear up and occur again within a few days
Keep out of reach of children
Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Cotrol Center right away.
Directions
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
Inactive ingredients cetyl alcohol, di-isopropyl adipate, dimethicone, glycerin, FORLAN-L (Contains: petrolatum, lanolin, hydrogenated coconut oil, sorbitan sesquioleate, stearyl alcohol, and cetyl alcohol), mineral oil, polyoxyl 40 stearate, potassium sorbate, povidone, purified water, sorbic acid, stearic acid, and trolamine
Label text from the FDA structured product label by Ferndale Laboratories, Inc. (revised Dec 17, 2024). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Pramoxine Hydrochloride in 1 product
DerMend Moisturizing Anti-Itch NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 0496-0586 | Pramoxine Hydrochloride 10 mg/mL Lotion | Ferndale Laboratories, Inc. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is DerMend Moisturizing Anti-Itch used for?
Use for the temporary relief of itching associated with minor skin irritations
Who makes DerMend Moisturizing Anti-Itch?
DerMend Moisturizing Anti-Itch is listed by 1 labeler in the FDA NDC directory, including Ferndale Laboratories, Inc..