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: BENZETHONIUM CHLORIDE; ALLANTOIN
Active strength: 1.2; .5 mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZETHONIUM CHLORIDE	1.2 mg/mL
ALLANTOIN	.5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
PH41D05744	Internal UNII lookup
344S277G0Z	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
25c6ada8-4a16-0896-e063-6294a90a0fdb	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-9655-10	Walgreens Advanced Wound Hydrogel	1 in 1 CARTON	GEL	1		4
0363-9655-10	Walgreens Advanced Wound Hydrogel	87 mL in 1 TUBE	GEL	87		4

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 22 of 22 · 424 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Family Wellness Antiseptic and Pain Relief	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE	FRONT PHARMACEUTICAL PLC	cb7fdcde-2bd8-4834-ba4e-4d6fd1512599	2023-10-26	Warnings	Exact identifier application number: M004
GENUINE FIRST AID Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Nantong Health & Beyond Hygienic Products Inc.	23abfe12-5b50-4b49-878e-4fcdb6c341fd	2023-10-19	Warnings	Exact identifier application number: M004
EVERLIT CARE Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Nantong Health & Beyond Hygienic Products Inc.	f4921508-c32f-426f-a2f0-16c3acbd4713	2023-10-14	Warnings	Exact identifier application number: M004
Cuadriderma	BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE	ProMex LLC	4fa99b96-ab4b-4523-82bc-343dbaf39fb6	2022-01-25	Warnings	Exact identifier application number: M004

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
PH41D05744	BENZETHONIUM CHLORIDE	121-54-0	BENZETHONIUM CHLORIDE
344S277G0Z	ALLANTOIN	97-59-6	ALLANTOIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
0363-9655-10	00363965510	1 TUBE in 1 CARTON (0363-9655-10) / 87 mL in 1 TUBE	1 tube	2025-02-28	No	No	Current