ULTIMATE DAILY FACE WASH- salicylic acid cream

Ultimate Daily Face Wash by

Drug Labeling and Warnings

Ultimate Daily Face Wash by is a Otc medication manufactured, distributed, or labeled by Dolgencorp Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment

Treatment Indications

• for the treatment of acne

Warnings

For external use only.

Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

Keep Out of Reach of Children.

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

Avoid contact with eyes.

If contact occurs, flush thoroughly with water.

Directions

• Wet face
• Dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area
• Rinse thoroughly with warm water and pat dry
• For best results, use twice daily

Inactive Ingredients

water, sodium cocoyl isethionate, stearic acid, coconut acid, sodium isethionate, sodium chloride, cetearyl alcohol, sodium hydroxide, glycerin, laureth-3, phenoxyethanol, methylparaben, ethylparaben, butylparaben, propylparaben, isobutylparaben, DMDM hydantoin, fragrance, disodium EDTA, lavandula stoechas extract, helichrysum italicum extract, cistus monspeliensis extract, caramel.

Questions or comments?

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Package/Label Principal Display Panel

DG™beauty Ultimate Daily Face Wash
Salicylic Acid 2.0%

• Fight acne 100%
• Dermatologically tested

Compare to Clearasil Ultra®
Daily Face Wash Ingredients*

6.78 FL OZ (200 mL)

*This product is not manufactured or distributed by Reckitt Bencloser, owner of the registered trademark Clearasil Ultra®

DISTRIBUTED BY:
DOLGENCORP, LLC
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072

MADE IN ISRAEL

Carton Label

INGREDIENTS AND APPEARANCE

ULTIMATE DAILY FACE WASH 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-333
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
LAURETH-3 (UNII: F32E4CB0UJ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CARAMEL (UNII: T9D99G2B1R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
CISTUS MONSPELIENSIS LEAF (UNII: 1IE70KNO43)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-333-11	1 in 1 CARTON
1		200 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	07/20/2013

Labeler - Dolgencorp Inc. (068331990)