Sheer Tint Mineral SPF Serum - Light Light

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Sheer Tint Mineral SPF Serum - Light Light
Generic name: ZINC OXIDE
Manufacturer: Mineral Fusion brands
Product type: HUMAN OTC DRUG
SPL set ID: ac6fdc35-82f8-4805-875e-2aa91aedec6f
SPL ID: fa25c6ac-ed84-4cef-83f5-1b4c1d332be0
Version: 1
Effective date: 2025-02-14
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:41

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Sheer Tint Mineral SPF Serum - Tan Tan	openfda.brand_name
brand name		Sheer Tint Mineral SPF Serum - Medium Medium	openfda.brand_name
brand name		Sheer Tint Mineral SPF Serum - Light Light	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Mineral Fusion brands	openfda.manufacturer_name
ndc	package	55789-2503-6	openfda.package_ndc
ndc	package	55789-2501-4	openfda.package_ndc
ndc	package	55789-2502-2	openfda.package_ndc
ndc	package	55789-2501-1	openfda.package_ndc
ndc	package	55789-2502-5	openfda.package_ndc
ndc	package	55789-2503-3	openfda.package_ndc
ndc	product	55789-2503	openfda.product_ndc
ndc	product	55789-2501	openfda.product_ndc
ndc	product	55789-2502	openfda.product_ndc
ndc11	package	55789250104	derived:openfda.package_ndc
ndc11	package	55789250205	derived:openfda.package_ndc
ndc11	package	55789250101	derived:openfda.package_ndc
ndc11	package	55789250306	derived:openfda.package_ndc
ndc11	package	55789250202	derived:openfda.package_ndc
ndc11	package	55789250303	derived:openfda.package_ndc
spl id		fa25c6ac-ed84-4cef-83f5-1b4c1d332be0	id
spl set id		ac6fdc35-82f8-4805-875e-2aa91aedec6f	set_id
unii		SOI2LOH54Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use on damaged or broken skin When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.