Package 59062-1229-1

Brand: babyganics sunscreen 30 spf

Generic: zinc oxide, octinoxate, and octisalate
NDC Package

Package Facts

Identity

Package NDC 59062-1229-1
Digits Only 5906212291
Product NDC 59062-1229
Description

177 mL in 1 BOTTLE, DISPENSING (59062-1229-1)

Marketing

Marketing Status
Discontinued 2026-12-31
Brand babyganics sunscreen 30 spf
Generic zinc oxide, octinoxate, and octisalate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "288cb5ff-0e3f-40de-8e46-3424f6d03c2c", "openfda": {"upc": ["0813277012290"], "unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["391a4ec3-b65b-4dbe-bc8f-cb67514c8ef1"], "manufacturer_name": ["KAS Direct LLC dba BabyGanics"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, DISPENSING (59062-1229-1)", "package_ndc": "59062-1229-1", "marketing_end_date": "20261231", "marketing_start_date": "20130621"}], "brand_name": "BabyGanics Sunscreen 30 SPF", "product_id": "59062-1229_288cb5ff-0e3f-40de-8e46-3424f6d03c2c", "dosage_form": "SPRAY", "product_ndc": "59062-1229", "generic_name": "ZINC OXIDE, OCTINOXATE, and OCTISALATE", "labeler_name": "KAS Direct LLC dba BabyGanics", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BabyGanics Sunscreen", "brand_name_suffix": "30 SPF", "active_ingredients": [{"name": "OCTINOXATE", "strength": "50 mg/mL"}, {"name": "OCTISALATE", "strength": "40 mg/mL"}, {"name": "ZINC OXIDE", "strength": "112 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20130621"}