Package 60232-0035-1

Brand: private label spf 50 80 min water resistant

Generic: homosalate, octisalate, zinc oxide sunscreen
NDC Package

Package Facts

Identity

Package NDC 60232-0035-1
Digits Only 6023200351
Product NDC 60232-0035
Description

1000 g in 1 TUBE (60232-0035-1)

Marketing

Marketing Status
Marketed Since 2020-12-01
Brand private label spf 50 80 min water resistant
Generic homosalate, octisalate, zinc oxide sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "6a3535ae-574f-48d8-bfc0-5b38f54c93ee", "openfda": {"unii": ["V06SV4M95S", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["8849fa88-24c8-410d-b16e-60da38288f98"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 g in 1 TUBE (60232-0035-1)", "package_ndc": "60232-0035-1", "marketing_start_date": "20201201"}], "brand_name": "Private Label SPF 50 80 min Water Resistant", "product_id": "60232-0035_6a3535ae-574f-48d8-bfc0-5b38f54c93ee", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0035", "generic_name": "homosalate, octisalate, zinc oxide sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label SPF 50 80 min Water Resistant", "active_ingredients": [{"name": "HOMOSALATE", "strength": "100 g/1000g"}, {"name": "OCTISALATE", "strength": "50 g/1000g"}, {"name": "ZINC OXIDE", "strength": "165 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}