Package 84891-2185-1

Brand: daily essential face moisturizer

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84891-2185-1
Digits Only 8489121851
Product NDC 84891-2185
Description

60 mL in 1 TUBE (84891-2185-1)

Marketing

Marketing Status
Marketed Since 2024-12-09
Brand daily essential face moisturizer
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43cc543f-a1c2-4f7d-e063-6394a90af35c", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["2a92edc1-04ac-3eda-e063-6294a90ad46d"], "manufacturer_name": ["Solarium Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 TUBE (84891-2185-1)", "package_ndc": "84891-2185-1", "marketing_start_date": "20241209"}], "brand_name": "Daily Essential Face Moisturizer", "product_id": "84891-2185_43cc543f-a1c2-4f7d-e063-6394a90af35c", "dosage_form": "LOTION", "product_ndc": "84891-2185", "generic_name": "Zinc Oxide", "labeler_name": "Solarium Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daily Essential Face Moisturizer", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "132 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241209", "listing_expiration_date": "20261231"}