OTC Medication Information: O HUI WHITE EXTREME CELLIGHT

O HUI WHITE EXTREME CELLIGHT — protocatechualdehyde cream
LG Household and Healthcare, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

PROTOCATECHUALDEHYDE 0.032%

Whitening cream

Stop use if rash or irritation develops and lasts.

Keep out of eyes. Rinse with water to remove.

Use to whiten skin.

Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

WATER, DIPROPYLENE GLYCOL, CYCLOPENTASILOXANE, GLYCERIN, MEDIUM-CHAIN TRIGLYCERIDES, NEOPENTYL GLYCOL DICAPRATE, TREHALOSE, SQUALANE, 1,2-HEXANEDIOL, GLYCERYL STEARATE, DIMETHICONE, PANTHENOL, ALCOHOL, PHENOXYETHANOL, COPPER, ALPHA-TOCOPHEROL, EDETATE TRISODIUM, TROLAMINE, SODIUM METABISULFITE.

OHUI
WHITE EXTREME

CELLIGHT CREAM

White Extreme Cellight Cream
(click image for full-size original)

Use as needed to whiten skin.

O HUI WHITE EXTREME CELLIGHT
protocatechualdehyde cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-507
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PROTOCATECHUALDEHYDE (PROTOCATECHUALDEHYDE) PROTOCATECHUALDEHYDE 0.032 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
DIPROPYLENE GLYCOL
TROLAMINE
MEDIUM-CHAIN TRIGLYCERIDES
CYCLOMETHICONE 5
GLYCERYL MONOSTEARATE
NEOPENTYL GLYCOL DICAPRATE
TREHALOSE
SQUALANE
1,2-HEXANEDIOL
DIMETHICONE
PHENOXYETHANOL
ALPHA-TOCOPHEROL
COPPER
PANTHENOL
SODIUM METABISULFITE
ALCOHOL
EDETATE TRISODIUM
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53208-507-02 1 CONTAINER (CONTAINER) in 1 BOX contains a CONTAINER (53208-507-01)
1 NDC:53208-507-01 50 mL in 1 CONTAINER This package is contained within the BOX (53208-507-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 03/16/2011
Labeler — LG Household and Healthcare, Inc. (688276187)
Registrant — LG Household and Healthcare, Inc. (688276187)
Establishment
Name Address ID/FEI Operations
LG Household and Healthcare, Inc. 688276187 manufacture

Revised: 05/2012 LG Household and Healthcare, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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