DERMAMED- skin protectant ointment 
DermaRite Industries, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DermaMed

​Active ingredient

Aluminum Hydroxide Gel 2%

Purpose

Skin protectant

Uses

Dries the oozing and weeping of poison: ivy, oak, or sumac, or other skin irritations.

Warnings

For external use only.

Avoid contact with eyes. In case of contact, flush thoroughly with water.

Warnings

Stop and ask a doctor if

Warnings

Keep out of reach of children.

​In case of accidental ingestion contact a Physician or Poison Control Center right away.

Directions

Apply liberally to the affected area as needed or as directed by a physician.

Other information

Inactive ingredients

Petrolatum, Lanolin, Water, Propylene Glycol, Stearyl Alcohol, Calcium Carbonate, Magnesium Hydroxide, Zinc Chloride, DMDM Hydantoin, Methylparaben, Propylparaben, Sodium Laureth Sulfate, Lanolin Alcohol, Cholecalciferol, Zea Mays (Corn) Oil, Retinyl Palmitate, Citric Acid, Sodium Chloride

Questions?

Call 800-337-6296 Mon - Fri 9AM - 5PM EST.

DermaMed Package Label and Principal Display Panel

Package LabelCase Label

DERMAMED 
skin protectant ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61924-214
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
LANOLIN (UNII: 7EV65EAW6H)  
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)  
PROPYLENE GLYCOL 1-(2-METHYLBUTYRATE) (UNII: 9Q5W5G6461)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CORN OIL (UNII: 8470G57WFM)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PETROLATUM (UNII: 4T6H12BN9U)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61924-214-04106 g in 1 TUBE; Type 0: Not a Combination Product10/18/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34710/18/2016
Labeler - DermaRite Industries, LLC (883925562)
Registrant - DermaRite Industries, LLC (883925562)
Establishment
NameAddressID/FEIBusiness Operations
DermaRite Industries, LLC883925562manufacture(61924-214)

Revised: 1/2020
Document Id: 9c59a3bf-a4d4-2fdd-e053-2a95a90a1c67
Set id: 5bd4173d-8794-3d28-e053-2991aa0a06a9
Version: 2
Effective Time: 20200117
 
DermaRite Industries, LLC