Package 35192-050-17

Brand: Sunscreen

Generic: Zinc Oxide
NDC Package

Package Facts

Identity

Package NDC 35192-050-17
Digits Only 3519205017
Product NDC 35192-050
Description

61 g in 1 PACKAGE (35192-050-17)

Marketing

Marketing Status
Marketed Since 2022-07-31
Brand Sunscreen
Generic Zinc Oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4617e22b-cfbc-21eb-e063-6294a90a1c87", "openfda": {"upc": ["0810145820551"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["e4b9c21f-ac5f-dc73-e053-2a95a90a1aaa"], "manufacturer_name": ["CA-Botana International"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "61 g in 1 PACKAGE (35192-050-17)", "package_ndc": "35192-050-17", "marketing_start_date": "20220731"}], "brand_name": "Sunscreen", "product_id": "35192-050_4617e22b-cfbc-21eb-e063-6294a90a1c87", "dosage_form": "EMULSION", "product_ndc": "35192-050", "generic_name": "Zinc Oxide", "labeler_name": "CA-Botana International", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "12.81 g/12.81g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220731", "listing_expiration_date": "20261231"}