Replenishing Non Tinted 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: Replenishing Non Tinted Sunscreen
Generic name: TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer: Beauty Journey Studio LLC
Product type: HUMAN OTC DRUG
SPL set ID: 37385fc6-1cde-8aa6-e063-6294a90a6017
SPL ID: 458c1711-6dbc-19cf-e063-6394a90af8ad
Version: 2
Effective date: 2025-12-09
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:13:09

Harmonized routes table
Harmonized routes
TOPICAL

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Replenishing Non Tinted Sunscreen	openfda.brand_name
generic name		TITANIUM DIOXIDE, ZINC OXIDE	openfda.generic_name
manufacturer name		Beauty Journey Studio LLC	openfda.manufacturer_name
ndc	package	85418-202-50	openfda.package_ndc
ndc	product	85418-202	openfda.product_ndc
ndc11	package	85418020250	derived:openfda.package_ndc
spl id		458c1711-6dbc-19cf-e063-6394a90af8ad	id
spl set id		37385fc6-1cde-8aa6-e063-6294a90a6017	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

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