Sheer Tint Mineral Sunscreen Broad Spectrum SPF 50 - Light/Medium Shade

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 Sunscreen Broad Spectrum SPF 50 - Light/Medium Shade
Generic name: SPF 50 SUNSCREEN BROAD SPECTRUM - LIGHT/MEDIUM SHADE
Manufacturer: Autumn Harp
Product type: HUMAN OTC DRUG
SPL set ID: fd6807e1-c8c0-b361-e053-6294a90aea0c
SPL ID: fd6807e1-c8c1-b361-e053-6294a90aea0c
Version: 1
Effective date: 2023-06-05
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:34

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Sheer Tint Mineral Sunscreen Broad Spectrum SPF 50 - Light/Medium Shade	openfda.brand_name
brand name		Sheer Tint Mineral Sunscreen Broad Spectrum SPF 50 - Medium/Deep Shade	openfda.brand_name
generic name		SPF 50 SUNSCREEN BROAD SPECTRUM - MEDIUM/DEEP SHADE	openfda.generic_name
generic name		SPF 50 SUNSCREEN BROAD SPECTRUM - LIGHT/MEDIUM SHADE	openfda.generic_name
manufacturer name		Autumn Harp	openfda.manufacturer_name
ndc	package	51514-0362-1	openfda.package_ndc
ndc	package	51514-0361-1	openfda.package_ndc
ndc	product	51514-0361	openfda.product_ndc
ndc	product	51514-0362	openfda.product_ndc
ndc11	package	51514036201	derived:openfda.package_ndc
ndc11	package	51514036101	derived:openfda.package_ndc
spl id		fd6807e1-c8c1-b361-e053-6294a90aea0c	id
spl set id		fd6807e1-c8c0-b361-e053-6294a90aea0c	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	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

For external use only Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right awy 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

Reported adverse events (FAERS/openFDA)#

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