ZO SKIN HEALTH PIGMENT CONTROL PLUS BLENDING CREME HYDROQUINONE- hydroquinone lotion

ZO Skin Health Pigment Control Plus Blending Creme Hydroquinone by

Drug Labeling and Warnings

ZO Skin Health Pigment Control Plus Blending Creme Hydroquinone by is a Otc medication manufactured, distributed, or labeled by ZO Skin Health, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Hydroquinone, 2%

Purpose

Skin Lightener

Uses

For the gradual fading of (or lightens) dark (or brownish) discolorations in the skin such as freckles, age spots, pigment in the skin that may occur in pregnancy or from the use of oral contraceptives.

Warnings

For external use only.

Avoid contact with eyes.

Do not use on children under 12 years of age unless directed by a doctor.

Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor.

Keep out of reach of children.

If swallowed, seek medical help or contact a Poison Control Center right away.

Directions

• Adults: Apply a small amount as a thin layer on the affected area twice daily, or use as directed by a doctor. If no improvement is seen after 3 months of treatment, use of this product should be discontinued. Lightening effect of this product may not be noticeable when used on very dark skin.
• Children under 12 years of age: do not use unless directed by a doctor.
• Sun exposure should be limited by using a sunscreen agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

Other Information

• Store at a controlled room temperature: 15°-30°C (59°-86°F), away from direct sunlight.

Inactive Ingredients

Aqua/Water/Eau, Ascorbic Acid, Ascorbyl Palmitate, Beta-Glucan, Caprylyl Glycol, Cetyl Alcohol, Chlorphenesin, Dioscorea Villosa (Wild Yam) Root Extract, Disodium EDTA, Ethylhexyl Palmitate, Glycerin, Glycolic Acid, Palmitic Acid, Phenoxyethanol, Phenyl Trimethicone, Quillaja Saponaria Bark Extract, Smilax Aristolochiifolia Root Extract, Sodium Hydroxide, Sodium Lauryl Sulfate, Sodium Metabisulfite, Sodium Sulfite, Stearyl Alcohol, Tocopheryl Acetate, Yucca Schidigera Root Extract

Questions?

5 Technology Dr. Irvine, CA 92618

SPL UNCLASSIFIED SECTION

Dist. by ZO Skin Health, Inc. Irvine, CA 92618

PRINCIPAL DISPLAY PANEL - 80 mL Bottle Carton

ZO® SKIN HEALTH
BY ZEIN OBAGI MD

NDC: 42851-039-80

PIGMENT CONTROL +
BLENDING CRÈME
2% Hydroquinone

80 mL / 2.7 Fl. Oz.

INGREDIENTS AND APPEARANCE

ZO SKIN HEALTH PIGMENT CONTROL PLUS BLENDING CREME HYDROQUINONE 
hydroquinone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42851-039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hydroquinone (UNII: XV74C1N1AE) (Hydroquinone - UNII:XV74C1N1AE)	Hydroquinone	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Ascorbic Acid (UNII: PQ6CK8PD0R)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Caprylyl Glycol (UNII: 00YIU5438U)
Cetyl Alcohol (UNII: 936JST6JCN)
Chlorphenesin (UNII: I670DAL4SZ)
DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
Ethylhexyl Palmitate (UNII: 2865993309)
Glycerin (UNII: PDC6A3C0OX)
Glycolic Acid (UNII: 0WT12SX38S)
Palmitic Acid (UNII: 2V16EO95H1)
Phenoxyethanol (UNII: HIE492ZZ3T)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Quillaja Saponaria Bark (UNII: 8N0K3807ZW)
Smilax Aristolochiifolia Root (UNII: NR100Y25G0)
Sodium Hydroxide (UNII: 55X04QC32I)
Sodium Lauryl Sulfate (UNII: 368GB5141J)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM SULFITE (UNII: VTK01UQK3G)
Stearyl Alcohol (UNII: 2KR89I4H1Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Yucca Schidigera Root (UNII: E2H9ET15AT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42851-039-80	1 in 1 CARTON	01/11/2019
1		80 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part358A	01/11/2019

Labeler - ZO Skin Health, Inc. (826468527)

Establishment
Name	Address	ID/FEI	Business Operations
PureTek Corporation		785961046	ANALYSIS(42851-039) , LABEL(42851-039) , MANUFACTURE(42851-039) , PACK(42851-039) , RELABEL(42851-039) , REPACK(42851-039)