Package 54108-8111-1

Brand: scar gel spf 35

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 54108-8111-1
Digits Only 5410881111
Product NDC 54108-8111
Description

1 TUBE in 1 BOX (54108-8111-1) / 43 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-07-15
Brand scar gel spf 35
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "04ff8c03-d928-4bfd-88d5-3bf14b9da3c9", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["8cd263aa-a54b-4c55-b3e2-6f6763987d4a"], "manufacturer_name": ["derma e"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (54108-8111-1)  / 43 g in 1 TUBE", "package_ndc": "54108-8111-1", "marketing_start_date": "20200715"}], "brand_name": "Scar Gel SPF 35", "product_id": "54108-8111_04ff8c03-d928-4bfd-88d5-3bf14b9da3c9", "dosage_form": "CREAM", "product_ndc": "54108-8111", "generic_name": "Zinc Oxide", "labeler_name": "derma e", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Scar Gel", "brand_name_suffix": "SPF 35", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "117 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200715", "listing_expiration_date": "20261231"}