Package 78863-1270-1

Brand: deflame

Generic: allantoin
NDC Package

Package Facts

Identity

Package NDC 78863-1270-1
Digits Only 7886312701
Product NDC 78863-1270
Description

1 TUBE in 1 CARTON (78863-1270-1) / 50 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-10-01
Brand deflame
Generic allantoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2b739f1b-7b76-4851-a368-a52fd2b7c38e", "openfda": {"unii": ["344S277G0Z"], "rxcui": ["241509"], "spl_set_id": ["2628bd73-0ca9-497b-bcd9-088444cd62be"], "manufacturer_name": ["Noon Aesthetics M.R. Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (78863-1270-1)  / 50 mL in 1 TUBE", "package_ndc": "78863-1270-1", "marketing_start_date": "20231001"}], "brand_name": "DeFlame", "product_id": "78863-1270_2b739f1b-7b76-4851-a368-a52fd2b7c38e", "dosage_form": "CREAM", "product_ndc": "78863-1270", "generic_name": "ALLANTOIN", "labeler_name": "Noon Aesthetics M.R. Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DeFlame", "active_ingredients": [{"name": "ALLANTOIN", "strength": "5 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}