Package 84444-506-00

Brand: guidance to glow tru spf 35

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84444-506-00
Digits Only 8444450600
Product NDC 84444-506
Description

1 TUBE in 1 BOX (84444-506-00) / 50 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-06-12
Brand guidance to glow tru 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": "1bb558bf-848a-1991-e063-6394a90a03d8", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["21b4747b-b173-43c9-b0d4-1dbba5775ff8"], "manufacturer_name": ["GUIDANCE TO GLOW SKIN CARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (84444-506-00)  / 50 mL in 1 TUBE", "package_ndc": "84444-506-00", "marketing_start_date": "20240612"}], "brand_name": "GUIDANCE TO GLOW TRU SPF 35", "product_id": "84444-506_1bb558bf-848a-1991-e063-6394a90a03d8", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "84444-506", "generic_name": "ZINC OXIDE", "labeler_name": "GUIDANCE TO GLOW SKIN CARE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GUIDANCE TO GLOW TRU SPF 35", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "120 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240612", "listing_expiration_date": "20261231"}