Package 0363-9655-10

Brand: walgreens advanced wound hydrogel

Generic: allantoin, benzethonium chloride
NDC Package

Package Facts

Identity

Package NDC 0363-9655-10
Digits Only 0363965510
Product NDC 0363-9655
Product ID 0363-9655_32459223-14c8-a1d7-e063-6394a90a37ba
Description

1 TUBE in 1 CARTON (0363-9655-10) / 87 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-02-28
Brand walgreens advanced wound hydrogel
Generic allantoin, benzethonium chloride
Sample Package No

Linked Drug Pages (1)

Walgreens Advanced Wound Hydrogel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "32459223-14c8-a1d7-e063-6394a90a37ba", "openfda": {"upc": ["0311917060002"], "unii": ["344S277G0Z", "PH41D05744"], "spl_set_id": ["25c6ada8-4a16-0896-e063-6294a90a0fdb"], "manufacturer_name": ["WALGREEN COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0363-9655-10)  / 87 mL in 1 TUBE", "package_ndc": "0363-9655-10", "marketing_start_date": "20250228"}], "brand_name": "Walgreens Advanced Wound Hydrogel", "product_id": "0363-9655_32459223-14c8-a1d7-e063-6394a90a37ba", "dosage_form": "GEL", "product_ndc": "0363-9655", "generic_name": "Allantoin, Benzethonium Chloride", "labeler_name": "WALGREEN COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Walgreens Advanced Wound Hydrogel", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".5 mg/mL"}, {"name": "BENZETHONIUM CHLORIDE", "strength": "1.2 mg/mL"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250228", "listing_expiration_date": "20261231"}