rite aid scar
Generic: allantoin 0.5%
Labeler: rite aidDrug Facts
Product Profile
Brand Name
rite aid scar
Generic Name
allantoin 0.5%
Labeler
rite aid
Dosage Form
GEL
Routes
Active Ingredients
allantoin .5 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
11822-1297
Product ID
11822-1297_2cb5ff15-1539-4665-e063-6294a90a811c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2022-09-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118221297
Hyphenated Format
11822-1297
Supplemental Identifiers
RxCUI
UPC
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
rite aid scar (source: ndc)
Generic Name
allantoin 0.5% (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 g/100g
Packaging
- 1 TUBE in 1 BOX (11822-1297-1) / 19.8 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": "2cb5ff15-1539-4665-e063-6294a90a811c", "openfda": {"upc": ["0011822661027"], "unii": ["344S277G0Z"], "rxcui": ["1442087"], "spl_set_id": ["fd152c8f-6df5-1236-e053-6394a90a865d"], "manufacturer_name": ["Rite Aid"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (11822-1297-1) / 19.8 g in 1 TUBE", "package_ndc": "11822-1297-1", "marketing_start_date": "20220915"}], "brand_name": "Rite Aid Scar", "product_id": "11822-1297_2cb5ff15-1539-4665-e063-6294a90a811c", "dosage_form": "GEL", "product_ndc": "11822-1297", "generic_name": "Allantoin 0.5%", "labeler_name": "Rite Aid", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rite Aid Scar", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".5 g/100g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}