Package 73676-217-02

Brand: abib heartleaf mild sunscreen relief tube

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 73676-217-02
Digits Only 7367621702
Product NDC 73676-217
Description

1 TUBE in 1 CARTON (73676-217-02) / 50 mL in 1 TUBE (73676-217-01)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand abib heartleaf mild sunscreen relief tube
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "34965587-c9b8-4066-e063-6394a90ab424", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["34965587-c9b7-4066-e063-6394a90ab424"], "manufacturer_name": ["FOURCOMPANY CO., LTD."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (73676-217-02)  / 50 mL in 1 TUBE (73676-217-01)", "package_ndc": "73676-217-02", "marketing_start_date": "20250501"}], "brand_name": "Abib Heartleaf mild sunscreen Relief tube", "product_id": "73676-217_34965587-c9b8-4066-e063-6394a90ab424", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "73676-217", "generic_name": "Zinc Oxide", "labeler_name": "FOURCOMPANY CO., LTD.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Abib Heartleaf mild sunscreen Relief tube", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "19.32 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}