Package 51352-999-11

Brand: fusidyne derma trouble zinc calming sunscreen

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 51352-999-11
Digits Only 5135299911
Product NDC 51352-999
Product ID 51352-999_46457c78-74d7-ea6a-e063-6294a90a24ac
Description

96 TUBE in 1 CARTRIDGE (51352-999-11) / 50 mL in 1 TUBE (51352-999-10)

Marketing

Marketing Status
Marketed Since 2026-01-01
Brand fusidyne derma trouble zinc calming sunscreen
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

FUSIDYNE DERMA TROUBLE Zinc Calming Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "46457c78-74d7-ea6a-e063-6294a90a24ac", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["46457c78-74d6-ea6a-e063-6294a90a24ac"], "manufacturer_name": ["DONG WHA PHARM. CO., LTD."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "96 TUBE in 1 CARTRIDGE (51352-999-11)  / 50 mL in 1 TUBE (51352-999-10)", "package_ndc": "51352-999-11", "marketing_start_date": "20260101"}], "brand_name": "FUSIDYNE DERMA TROUBLE Zinc Calming Sunscreen", "product_id": "51352-999_46457c78-74d7-ea6a-e063-6294a90a24ac", "dosage_form": "LOTION", "product_ndc": "51352-999", "generic_name": "Zinc Oxide", "labeler_name": "DONG WHA PHARM. CO., LTD.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FUSIDYNE DERMA TROUBLE Zinc Calming Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "8.463275 g/50mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260101", "listing_expiration_date": "20271231"}