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 Wakefern Food Corp. 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 massage 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, decyl glucoside, Zea mays (corn) kernel meal, cetearyl alcohol, cetyl alcohol, triethanolamine, cocamidopropyl betaine, glyceryl stearate, PEG-100 stearate, Prunus armeniaca (apricot) fruit extract, cetyl acetate, ceteareth-20, carbomer, polysorbate 60, acetylated lanolin alcohol, fragrance, PPG-2 methyl ether, phenethyl alcohol, methylisothiazolinone, titanium dioxide

SPL UNCLASSIFIED SECTION

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

DISTRIBUTED BY
WAKEFERN FOOD CORP
5000 RIVERSIDE DRIVE
KEASBEY, NJ 08832
1-800-SHOPRITE
www.shoprite.com

Principal Display Panel

ShopRite

Apricot Scrub acne medication

blemish + blackhead control

for oily skin

Oil free

2% salicylic acid

sulfate and paraben free

exfoliates gently to remove dirt, oil and dead skin cells that can clog pores

NET WT 6 OZ (170 g)

041.005/041AF-AG

INGREDIENTS AND APPEARANCE

MEDICATED APRICOT SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41190-041
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)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CORN GRAIN (UNII: C1Z9U7094Z)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
TROLAMINE (UNII: 9O3K93S3TK)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
APRICOT (UNII: 269CJD5GZ9)
CETYL ACETATE (UNII: 4Q43814HXS)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
POLYSORBATE 60 (UNII: CAL22UVI4M)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
.ALPHA.-ISOBUTYLPHENETHYL ALCOHOL (UNII: 2SBL0E1I0N)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41190-041-30	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 final	part333D	12/14/2010

Labeler - Wakefern Food Corp (069722418)