TALLOW SUNSCREEN

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: TALLOW SUNSCREEN
Generic name: NON-NANO ZINC OXIDE
Manufacturer: FOUNDATION COMMERCE INC
Product type: HUMAN OTC DRUG
SPL set ID: 363e38bf-b4b4-dcc4-e063-6294a90a5d2f
SPL ID: 363e38bf-b4b5-dcc4-e063-6294a90a5d2f
Version: 1
Effective date: 2025-05-28
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 06:19:13

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		TALLOW SUNSCREEN	openfda.brand_name
generic name		NON-NANO ZINC OXIDE	openfda.generic_name
manufacturer name		FOUNDATION COMMERCE INC	openfda.manufacturer_name
ndc	package	85739-001-01	openfda.package_ndc
ndc	product	85739-001	openfda.product_ndc
ndc11	package	85739000101	derived:openfda.package_ndc
spl id		363e38bf-b4b5-dcc4-e063-6294a90a5d2f	id
spl set id		363e38bf-b4b4-dcc4-e063-6294a90a5d2f	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

For external use only on damaged or broken skin Keep out of eyes. Rinse with water to remowe. Ask a doctor if rash occurs. lf product is 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.