HQLA- hydroquinone cream

HQLA by

Drug Labeling and Warnings

HQLA by is a Otc medication manufactured, distributed, or labeled by Private Label Skin Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Hydroquinone 2%

Purpose

Skin Lightener

INDICATIONS & USAGE

Use Lightens dark discolorations in skin such as: freckles, age and liver spots or pigment in the skin that may occur in the skin.

WARNINGS

Warnings For external use only.

When using this product keep out of eyes. Rinse with water to remove. Stop use and ask physician if rash occurs.

If pregnant or breast-feeding Ask a physician before use.

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

DOSAGE & ADMINISTRATION

Directions Apply sparingly over face and neck, avoiding eye area. Can be used once a day at bedtime or as directed by physician.

Sunburn Alert This product may increase your skins sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product.

INACTIVE INGREDIENT

Inactive Ingredients Water, Ethylhexyl Methoxycinnamate, Cetearyl Alcohol, Propylene Glycol, C12-15 Alkyl Benzoate, Cetyl Alcohol, Sorbitan Stearate, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Glycol Distearate, Potassium Cetyl Phosphate, Sodium Metabisulfite, Triticum Vulgare (Wheat) Germ Oil, Helianthus Annuus (Sunflower) Seed Oil, Xanthan Gum, Lactic Acid, Methylparaben, Allantoin, BHT, Imidazolidinyl Urea, Tetrasodium EDTA, Propylparaben

SPL UNCLASSIFIED SECTION

brand MD®

SKIN CARE

AGE DEFENSE

medical grade

√ Lightens overall complexion, corrects uneven skin tone

√ Reduces melanin formation

brandMD®

Chatsworth, CA 91311

www.brandMD.com

Toll Free: (877) 252-7546

Made in USA

Packaging

INGREDIENTS AND APPEARANCE

HQLA 
hydroquinone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72957-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
OCTINOXATE (UNII: 4Y5P7MUD51)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CETYL ALCOHOL (UNII: 936JST6JCN)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
ISOHEXADECANE (UNII: 918X1OUF1E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
WHEAT GERM OIL (UNII: 14C97E680P)
SUNFLOWER OIL (UNII: 3W1JG795YI)
XANTHAN GUM (UNII: TTV12P4NEE)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
METHYLPARABEN (UNII: A2I8C7HI9T)
ALLANTOIN (UNII: 344S277G0Z)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
IMIDUREA (UNII: M629807ATL)
EDETATE SODIUM (UNII: MP1J8420LU)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72957-004-01	49 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358A	01/23/2020

Labeler - Private Label Skin Care (116996962)

Establishment
Name	Address	ID/FEI	Business Operations
Private Label Skin Care		116996962	relabel(72957-004)