ZO Skin Health Pigment Control Creme Hydroquinone

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: ZO Skin Health Pigment Control Creme Hydroquinone
Generic name: HYDROQUINONE
Manufacturer: ZO Skin Health, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 83e34a75-d20c-43ab-be31-f8fcafec46d0
SPL ID: 2d4578ad-1742-6f8f-e063-6294a90a3d1c
Version: 5
Effective date: 2025-02-03
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:32:42

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ZO Skin Health Pigment Control Creme Hydroquinone	openfda.brand_name
generic name		HYDROQUINONE	openfda.generic_name
manufacturer name		ZO Skin Health, Inc.	openfda.manufacturer_name
ndc	package	42851-037-30	openfda.package_ndc
ndc	package	42851-037-80	openfda.package_ndc
ndc	product	42851-037	openfda.product_ndc
ndc11	package	42851003780	derived:openfda.package_ndc
ndc11	package	42851003730	derived:openfda.package_ndc
rxcui		1235391	openfda.rxcui
spl id		2d4578ad-1742-6f8f-e063-6294a90a3d1c	id
spl set id		83e34a75-d20c-43ab-be31-f8fcafec46d0	set_id
unii		XV74C1N1AE	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 Keep out of reach of children. Contains Sodium Metabisulfite, a sulfite that may cause serious allergic-type reactions, including anaphylactic symptoms (e.g., hives, itching) and life-threatening or less-severe asthmatic episodes in certain susceptible persons. For external use only. Avoid contact with the eyes. Some users may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a physician. Do not use on children under 12 years of age unless directed by a physician. 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.