Package 61328-120-12

Brand: 911

Generic: allantoin
NDC Package

Package Facts

Identity

Package NDC 61328-120-12
Digits Only 6132812012
Product NDC 61328-120
Product ID 61328-120_471aac11-1c14-86fa-e063-6294a90a082e
Description

8.5 g in 1 TUBE (61328-120-12)

Marketing

Marketing Status
Marketed Since 2018-12-26
Brand 911
Generic allantoin
Sample Package No

Linked Drug Pages (1)

911 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "471aac11-1c14-86fa-e063-6294a90a082e", "openfda": {"unii": ["344S277G0Z"], "rxcui": ["1044541"], "spl_set_id": ["f28c251e-a91b-4ed4-8224-b47c345f982f"], "manufacturer_name": ["Skinfix, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (61328-120-11)", "package_ndc": "61328-120-11", "marketing_start_date": "20181226"}, {"sample": false, "description": "8.5 g in 1 TUBE (61328-120-12)", "package_ndc": "61328-120-12", "marketing_start_date": "20181226"}], "brand_name": "911", "product_id": "61328-120_471aac11-1c14-86fa-e063-6294a90a082e", "dosage_form": "OINTMENT", "product_ndc": "61328-120", "generic_name": "Allantoin", "labeler_name": "Skinfix, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "911", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".5 g/100g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181226", "listing_expiration_date": "20261231"}