SCARLIGHT MD- hydroquinone liquid

Scarlight MD by

Drug Labeling and Warnings

Scarlight MD by is a Otc medication manufactured, distributed, or labeled by Scarguard Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Hydroquinone 2%

Purpose

Skin Lightener

Uses

• lightens dark (brownish) discoloration in the skin such as age and liver spots

Warnings

For external use only

Do not use

• on children under 12 years of age.  Consult a doctor.
• on mucous membranes

When using this product

• mild irritation may occur
• avoid contact with eyes.  If contact occurs, rinse with water.

Stop use and ask a doctor if

• irritation becomes severe
• condition worsens

Keep out of reach of children.

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

Directions

• adults: brush a small amount twice daily. Rub in.
• limit sun exposure and use a sunscreen, a sun blocking agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring
• discontinue if symptoms persist for more than 3 months
• children under 12 years of age, consult a doctor before use

Other Information

• store at 15º to 30ºC (59 to 86ºF)
• keep bottle tightly closed or product will evaporate

Inactive Ingredients

retinoic acid, melatonin, MSM, BHT, na metabisulfite, arbutin, cystamine, licorice root, dandelion root, hydroxyanisole, ascorbic acid, hydroxypropylcellulose, kojic acid, azelaic acid, acetone, propylene glycol, ethyl alcohol (SDA), distilled water q.s.

Questions

call

1-877-566-5935

Carton 15mL

Carton 30mL

INGREDIENTS AND APPEARANCE

SCARLIGHT MD 
hydroquinone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64269-9902
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
Propylene Glycol (UNII: 6DC9Q167V3)
Alcohol (UNII: 3K9958V90M)
Acetone (UNII: 1364PS73AF)
Azelaic Acid (UNII: F2VW3D43YT)
Hydroxypropyl Cellulose (UNII: RFW2ET671P)
Ascorbic Acid (UNII: PQ6CK8PD0R)
Butylated Hydroxyanisole (UNII: REK4960K2U)
TARAXACUM OFFICINALE ROOT (UNII: 9DE5YCO0RU)
Licorice (UNII: 61ZBX54883)
Arbutin (UNII: C5INA23HXF)
Sodium Metabisulfite (UNII: 4VON5FNS3C)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Dimethyl Sulfone (UNII: 9H4PO4Z4FT)
Melatonin (UNII: JL5DK93RCL)
Tretinoin (UNII: 5688UTC01R)
Water (UNII: 059QF0KO0R)
Kojic Acid (UNII: 6K23F1TT52)
Cystamine (UNII: R110LV8L02)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64269-9902-8	30 mL in 1 BOTTLE, WITH APPLICATOR
2	NDC: 64269-9902-7	15 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358	11/01/2002

Labeler - Scarguard Labs, LLC (842204575)

Registrant - Scarguard Labs, LLC (842204575)