Package 72944-0001-1

Brand: kenaf wet wipe

Generic: allantoin
NDC Package

Package Facts

Identity

Package NDC 72944-0001-1
Digits Only 7294400011
Product NDC 72944-0001
Description

190 g in 1 POUCH (72944-0001-1)

Marketing

Marketing Status
Marketed Since 2017-04-09
Brand kenaf wet wipe
Generic allantoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "384bb90a-444d-547a-e063-6394a90a354b", "openfda": {"unii": ["344S277G0Z"], "spl_set_id": ["860f9cc5-a00e-7ccf-e053-2a91aa0a0782"], "manufacturer_name": ["MEDICELL BIO CO., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "190 g in 1 POUCH (72944-0001-1)", "package_ndc": "72944-0001-1", "marketing_start_date": "20170409"}], "brand_name": "Kenaf wet wipe", "product_id": "72944-0001_384bb90a-444d-547a-e063-6394a90a354b", "dosage_form": "LIQUID", "product_ndc": "72944-0001", "generic_name": "ALLANTOIN", "labeler_name": "MEDICELL BIO CO., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kenaf wet wipe", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".05 g/100g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20170409", "listing_expiration_date": "20261231"}