MEDICATED APRICOT SCRUB- salicylic acid gel

Medicated Apricot Scrub by

Drug Labeling and Warnings

Medicated Apricot Scrub by is a Otc medication manufactured, distributed, or labeled by Retail Business Services, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

When using this product

• skin irritation and dryness is more likely to occure if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out of reach of children.

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

Directions

• moisten face with water. Apply product with wet fingertips and masage over face. Rinse well and pat dry
• avoid contact with the eyes.  If contact occurs, flush thoroughly with water.

Other information

store at room temperature

Inactive ingredients

water, Juglans regia (walnut) shell powder, glyceryl stearate SE, glycerin, cetearyl alcohol, cetyl alcohol, decyl glucoside, Zea mays (corn) kernel meal, sodium hydroxide, cocamidopropyl betaine, glyceryl stearate, PEG-100 stearate, Prunus armeniaca (apricot) fruit extract, ceteareth-20, carbomer, polysorbate 60, fragrance, PPG-2 methyl ether, phenethyl alcohol, methylisothiazolinone, benzyl alcohol, limonene, titanium dioxide

Disclaimer

*This product is not manufactured or distributed by Unilever, distributor of St. Ives ®Blemish Control Apricot Scrub.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: 

ADUSA DISTRIBUTION, LLC

SALISBURY, NC 28147

For product questions or concerns, contact us at 1-833-992-3872

Quality guaranteed or your money back.

Principal display panel

CAREone ®

Compare to St. Ives ®Blemish Control Apricot Scrub*

APRICOT SCRUB

ACNE MEDICATION

Dermatologist Tested

• Paraben or Sulfates

NET WT 6 0Z (170 g)

INGREDIENTS AND APPEARANCE

MEDICATED APRICOT SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72476-044
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	19.8 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CORN GRAIN (UNII: C1Z9U7094Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
APRICOT (UNII: 269CJD5GZ9)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72476-044-30	170 g in 1 TUBE; Type 0: Not a Combination Product	12/14/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/14/2010

Labeler - Retail Business Services, LLC (967989935)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(72476-044)