Package 59899-010-01

Brand: youth 1 activating bb cream spf 30 light

Generic: zinc oxide, titanium dioxide
NDC Package

Package Facts

Identity

Package NDC 59899-010-01
Digits Only 5989901001
Product NDC 59899-010
Description

1 TUBE in 1 CARTON (59899-010-01) / 30 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-08-09
Brand youth 1 activating bb cream spf 30 light
Generic zinc oxide, titanium dioxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0949bf30-fab9-b9ff-e063-6394a90ad4dc", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["c9e05055-48ea-405d-b1d4-50b263d0dbf9"], "manufacturer_name": ["Shaklee Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59899-010-01)  / 30 mL in 1 TUBE", "package_ndc": "59899-010-01", "marketing_start_date": "20170809"}], "brand_name": "Youth 1 Activating BB Cream SPF 30 Light", "product_id": "59899-010_0949bf30-fab9-b9ff-e063-6394a90ad4dc", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "59899-010", "generic_name": "ZINC OXIDE, TITANIUM DIOXIDE", "labeler_name": "Shaklee Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Youth 1 Activating BB Cream SPF 30 Light", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "23.6 mg/mL"}, {"name": "ZINC OXIDE", "strength": "63 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170809", "listing_expiration_date": "20261231"}