WALGREENS ADVANCED WOUND HYDROGEL- allantoin, benzethonium chloride gel

Walgreens Advanced Wound Hydrogel by

Drug Labeling and Warnings

Walgreens Advanced Wound Hydrogel by is a Otc medication manufactured, distributed, or labeled by WALGREEN COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Allantoin (0.5%)

Benzethonium Chloride (0.12%)

Uses:

Temporarily protects minor cuts, scrapes, and burns
Temporarily protects and helps relieve chapped or cracked skin and lips
First aid to help decrease the risk of infection in minor cuts, scrapes and burns

Warnings:

For external use only

Ask a doctor before use if you have:

• Deep or puncture wounds
• deep cuts
• Animal bite
• Serious burns

Do not use:

• in the eyes
• over large areas of the body

When using this product:

• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• Apply only to the affected area.
• Avoid ingestion.

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.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions:

Adults and children 2 years of age & older:

• Clean minor cut, scrapes, or burns by thoroughly flushing the affected area with water or a wound cleanser and let air dry
• apply appropriate layer of the gel to cover the affected area
• may be covered with a sterile bandage
• apply 1 to 3 times daily

Children under 2 years of age:

• ask a doctor

Other information:

• Store at room temperature 68°F -77°F (20° to 25°C)
• Do not expose to excessive heat
• May discolor or stain certain fabrics

Inactive ingredients:

Acemannan Hydrogel from Aloe Vera, C13-14 Isoparaffin, Ethyl alcohol, Ethylhexylglycerin, Glycerin, Hydrastis Canadensis Dry Leaf Extract, Hydrastis Canadensis Root, Hydrolyzed Bovine Collagen, Panax Quinquefolius Root Extract, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Sodium Hyaluronate, Sodium Hydroxide, Water.

Package Labeling:

INGREDIENTS AND APPEARANCE

WALGREENS ADVANCED WOUND HYDROGEL 
allantoin, benzethonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9655
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	1.2 mg  in 1 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ACEMANNAN (UNII: UZ29E6L2X8)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
AMERICAN GINSENG (UNII: 8W75VCV53Q)
SODIUM ACRYLATE (UNII: 7C98FKB43H)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9655-10	1 in 1 CARTON	02/28/2025
1		87 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	02/28/2025

Labeler - WALGREEN COMPANY (008965063)

Registrant - WALGREEN COMPANY (008965063)