walgreens advanced scar gel
Generic: advanced scar gel
Labeler: walgreens companyDrug Facts
Product Profile
Brand Name
walgreens advanced scar gel
Generic Name
advanced scar gel
Labeler
walgreens company
Dosage Form
GEL
Routes
Active Ingredients
allantoin 5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
0363-2312
Product ID
0363-2312_fbca3a59-215c-4b21-845e-e175e345cf3a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2019-03-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03632312
Hyphenated Format
0363-2312
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
walgreens advanced scar gel (source: ndc)
Generic Name
advanced scar gel (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/g
Packaging
- 1 TUBE in 1 CARTON (0363-2312-07) / 20 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "fbca3a59-215c-4b21-845e-e175e345cf3a", "openfda": {"unii": ["344S277G0Z"], "rxcui": ["1442087"], "spl_set_id": ["2c040475-a124-485c-933e-66b452f5ab46"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0363-2312-07) / 20 g in 1 TUBE", "package_ndc": "0363-2312-07", "marketing_start_date": "20190326"}], "brand_name": "Walgreens Advanced Scar Gel", "product_id": "0363-2312_fbca3a59-215c-4b21-845e-e175e345cf3a", "dosage_form": "GEL", "product_ndc": "0363-2312", "generic_name": "Advanced Scar Gel", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Walgreens Advanced Scar Gel", "active_ingredients": [{"name": "ALLANTOIN", "strength": "5 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190326", "listing_expiration_date": "20261231"}