kinfield sunglow luminizing facial sunscreen broad spectrum spf 35

Generic: kinfield sunglow luminizing facial sunscreen broad spectrum spf 35

Labeler: kinfield, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name kinfield sunglow luminizing facial sunscreen broad spectrum spf 35
Generic Name kinfield sunglow luminizing facial sunscreen broad spectrum spf 35
Labeler kinfield, inc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

zinc oxide 20.3 g/100g

Manufacturer
Kinfield, Inc.

Identifiers & Regulatory

Product NDC 81750-050
Product ID 81750-050_472bab5b-ac3a-0fd7-e063-6394a90ad2d7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-08-14

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81750050
Hyphenated Format 81750-050

Supplemental Identifiers

UPC
0850007156121
UNII
SOI2LOH54Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name kinfield sunglow luminizing facial sunscreen broad spectrum spf 35 (source: ndc)
Generic Name kinfield sunglow luminizing facial sunscreen broad spectrum spf 35 (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20.3 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 PACKAGE (81750-050-06) / 60 g in 1 TUBE
source: ndc

Packages (1)

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

Ingredients (1)

zinc oxide (20.3 g/100g)

Linked Drug Pages (1)

Kinfield Sunglow Luminizing Facial Sunscreen Broad Spectrum SPF 35 ndc-match (0.9)

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"}