PROCURE DRYDROX- aluminum hydroxide gel 2% ointment

ProCure DryDrox by

Drug Labeling and Warnings

ProCure DryDrox by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Aluminum Hydroxide Gel 2%

Purpose

Skin Protectant

Uses

Uses

• Dries the oozing and weeping of poison ivy, oak and sumac

Directions

Directions

• Apply as needed
• Children under 6 months of age: ask a doctor

Inactive Ingredients

Calcium Carbonate, Cholecalciferol, Citric Acid, Ethylhexylglycerin, Glyceryl Monostearate, Glyceryl Stearate/ PEG-100 Stearate, Lanolin, Magnesium Hydroxide, Petrolatum, Phenoxyethanol, Propylene Glycol, Retinyl Palmitate, Sodium Chloride, Sodium Laureth Sulfate,Stearyl Alcohol, Water, Zea Mays Corn Oil, Zinc Chloride

Warnings

Warnings

For external use only

When using this product

When using this productdo not get into the eyes

Stop use and ask a doctor if

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

Keep out of reach of children

Keep out of reach of children.In case of accidental ingestion contact a physician or Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE DRYDROX 
aluminum hydroxide gel 2% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ZEA MAYS (CORN) OIL (UNII: 8470G57WFM)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LANOLIN (UNII: 7EV65EAW6H)
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CALCIUM CARBONATE (UNII: H0G9379FGK)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
PETROLATUM (UNII: 4T6H12BN9U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
RETINYL PALMITATE (UNII: 1D1K0N0VVC)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
WATER (UNII: 059QF0KO0R)
ZINC CHLORIDE (UNII: 86Q357L16B)

Product Characteristics
Color	white (White to off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-031-04	106 g in 1 TUBE; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/15/2025

Labeler - Twin Med LLC (009579330)