manuka honey extra strength
Generic: allantoin
Labeler: first honey llcDrug Facts
Product Profile
Brand Name
manuka honey extra strength
Generic Name
allantoin
Labeler
first honey llc
Dosage Form
GEL
Routes
Active Ingredients
allantoin 5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
81995-050
Product ID
81995-050_2d5e1f54-b018-fce5-e063-6394a90a76d7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2024-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81995050
Hyphenated Format
81995-050
Supplemental Identifiers
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
manuka honey extra strength (source: ndc)
Generic Name
allantoin (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/g
Packaging
- 1 TUBE in 1 CARTON (81995-050-01) / 21 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": "2d5e1f54-b018-fce5-e063-6394a90a76d7", "openfda": {"upc": ["0854056008356"], "unii": ["344S277G0Z"], "spl_set_id": ["b742585d-9a0c-489b-b268-590583cfabd1"], "manufacturer_name": ["First Honey LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (81995-050-01) / 21 g in 1 TUBE", "package_ndc": "81995-050-01", "marketing_start_date": "20240901"}], "brand_name": "Manuka Honey Extra Strength", "product_id": "81995-050_2d5e1f54-b018-fce5-e063-6394a90a76d7", "dosage_form": "GEL", "product_ndc": "81995-050", "generic_name": "ALLANTOIN", "labeler_name": "First Honey LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Manuka Honey Extra Strength", "active_ingredients": [{"name": "ALLANTOIN", "strength": "5 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}