Package 81995-050-01
Brand: manuka honey extra strength
Generic: allantoinPackage Facts
Identity
Package NDC
81995-050-01
Digits Only
8199505001
Product NDC
81995-050
Description
1 TUBE in 1 CARTON (81995-050-01) / 21 g in 1 TUBE
Marketing
Marketing Status
Brand
manuka honey extra strength
Generic
allantoin
Sample Package
No
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"}