Package 35192-044-01
Brand: Mineral Sunscreen
Generic: Zinc OxidePackage Facts
Identity
Package NDC
35192-044-01
Digits Only
3519204401
Product NDC
35192-044
Description
61 g in 1 TUBE (35192-044-01)
Marketing
Marketing Status
Brand
Mineral 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": "47e497ef-68f8-4404-e063-6394a90a0dac", "openfda": {"upc": ["0707060954921"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["c7929b18-76f5-af11-e053-2a95a90a183c"], "manufacturer_name": ["CA-Botana International"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "61 g in 1 TUBE (35192-044-01)", "package_ndc": "35192-044-01", "marketing_start_date": "20210815"}], "brand_name": "Mineral Sunscreen", "product_id": "35192-044_47e497ef-68f8-4404-e063-6394a90a0dac", "dosage_form": "EMULSION", "product_ndc": "35192-044", "generic_name": "Zinc Oxide", "labeler_name": "CA-Botana International", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "12.81 g/12.81g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210815", "listing_expiration_date": "20271231"}