5-IN-1 TINTED FACE SUNSCREEN - FAIR

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: 5-IN-1 TINTED FACE SUNSCREEN - FAIR
Generic name: ZINC OXIDE
Manufacturer: Synchronicity Spa, Inc. DBA Suntegrity
Product type: HUMAN OTC DRUG
SPL set ID: c0892856-cd12-4c1f-8420-866dbd0f8907
SPL ID: 2c5a7500-d9ee-4d1b-b79d-c7adb8e70faf
Version: 3
Effective date: 2025-06-04
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:26:58

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		5-IN-1 TINTED FACE SUNSCREEN - LIGHT	openfda.brand_name
brand name		5-IN-1 TINTED FACE SUNSCREEN - GOLDEN LIGHT	openfda.brand_name
brand name		5-IN-1 TINTED FACE SUNSCREEN - MEDIUM	openfda.brand_name
brand name		5-IN-1 TINTED FACE SUNSCREEN - FAIR	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Synchronicity Spa, Inc. DBA Suntegrity	openfda.manufacturer_name
ndc	package	69949-052-01	openfda.package_ndc
ndc	package	69949-051-01	openfda.package_ndc
ndc	package	69949-053-01	openfda.package_ndc
ndc	package	69949-054-01	openfda.package_ndc
ndc	product	69949-051	openfda.product_ndc
ndc	product	69949-054	openfda.product_ndc
ndc	product	69949-053	openfda.product_ndc
ndc	product	69949-052	openfda.product_ndc
ndc11	package	69949005101	derived:openfda.package_ndc
ndc11	package	69949005401	derived:openfda.package_ndc
ndc11	package	69949005301	derived:openfda.package_ndc
ndc11	package	69949005201	derived:openfda.package_ndc
spl id		2c5a7500-d9ee-4d1b-b79d-c7adb8e70faf	id
spl set id		c0892856-cd12-4c1f-8420-866dbd0f8907	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 Stop use and ask a doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove. 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.