Walgreens Advanced Wound Hydrogel

Product NDC
0363-9655
11-digit product format
003639655
Labeler code
0363
Product ID
0363-9655_32459223-14c8-a1d7-e063-6394a90a37ba
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin, Benzethonium Chloride
Dosage form
GEL
Route
TOPICAL
Labeler
WALGREEN COMPANY
Application
M004
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-28
Substance
ALLANTOIN; BENZETHONIUM CHLORIDE
Active strength
.5; 1.2 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Walgreens Advanced Wound Hydrogel
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALLANTOIN.5 mg/mL
BENZETHONIUM CHLORIDE1.2 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii344S277G0Z, PH41D05744

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9655-10Walgreens Advanced Wound Hydrogel1 in 1 CARTONGEL14
0363-9655-10Walgreens Advanced Wound Hydrogel87 mL in 1 TUBEGEL874

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0363-9655-10003639655101 TUBE in 1 CARTON (0363-9655-10) / 87 mL in 1 TUBE1 tube2025-02-28NoNoCurrent