Package 35192-051-01

Brand: Sunscreen

Generic: Zinc Oxide
NDC Package

Package Facts

Identity

Package NDC 35192-051-01
Digits Only 3519205101
Product NDC 35192-051
Product ID 35192-051_46199d8d-e20b-ce16-e063-6294a90ae329
Description

62.3 g in 1 PACKAGE (35192-051-01)

Marketing

Marketing Status
Marketed Since 2022-09-30
Brand Sunscreen
Generic Zinc Oxide
Sample Package No

Linked Drug Pages (1)

Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "46199d8d-e20b-ce16-e063-6294a90ae329", "openfda": {"upc": ["0196852191994"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["e74f7c79-59e2-f6e2-e053-2a95a90ad832"], "manufacturer_name": ["CA-Botana International"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "62.3 g in 1 PACKAGE (35192-051-01)", "package_ndc": "35192-051-01", "marketing_start_date": "20220930"}], "brand_name": "Sunscreen", "product_id": "35192-051_46199d8d-e20b-ce16-e063-6294a90ae329", "dosage_form": "EMULSION", "product_ndc": "35192-051", "generic_name": "Zinc Oxide", "labeler_name": "CA-Botana International", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "21 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}