Package 81750-050-06

Brand: kinfield sunglow luminizing facial sunscreen broad spectrum spf 35

Generic: kinfield sunglow luminizing facial sunscreen broad spectrum spf 35
NDC Package

Package Facts

Identity

Package NDC 81750-050-06
Digits Only 8175005006
Product NDC 81750-050
Description

1 TUBE in 1 PACKAGE (81750-050-06) / 60 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-08-14
Brand kinfield sunglow luminizing facial sunscreen broad spectrum spf 35
Generic kinfield sunglow luminizing facial sunscreen broad spectrum spf 35
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "472bab5b-ac3a-0fd7-e063-6394a90ad2d7", "openfda": {"upc": ["0850007156121"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["cbdfd0ae-514b-4b53-98ad-4270163bd0df"], "manufacturer_name": ["Kinfield, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 PACKAGE (81750-050-06)  / 60 g in 1 TUBE", "package_ndc": "81750-050-06", "marketing_start_date": "20240814"}], "brand_name": "Kinfield Sunglow Luminizing Facial Sunscreen Broad Spectrum SPF 35", "product_id": "81750-050_472bab5b-ac3a-0fd7-e063-6394a90ad2d7", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "81750-050", "generic_name": "Kinfield Sunglow Luminizing Facial Sunscreen Broad Spectrum SPF 35", "labeler_name": "Kinfield, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kinfield Sunglow Luminizing Facial Sunscreen Broad Spectrum SPF 35", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "20.3 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240814", "listing_expiration_date": "20261231"}