MEDICATED APRICOT SCRUB- salicylic acid gel 
United Natural Foods, Inc. dba UNFI

----------

Equaline 041.006/041AK
Medicated Apricot Scrub

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

When using this product

Keep out of reach of children.

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

Directions

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

Questions?

Call 1-855-423-2630

Disclaimer

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

Adverse reaction

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

PROVIDENCE, RI 02908 USA

Principal Panel Display

EQUALINE®

COMPARE TO St. Ives Blemish Control Apricot Scrub*

BLEMISH AND BLACKHEAD CONTROL

Medicated Apricot Scrub

salicylic acid acne medication with natural exfoliants

dermatologist tested

exfoliates to prevent blemishes and cleanse pores

NET WT 6 0Z (170 g)

image description

MEDICATED APRICOT SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-041
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID19.8 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-041-30170 g in 1 TUBE; Type 0: Not a Combination Product07/06/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00607/06/2015
Labeler - United Natural Foods, Inc. dba UNFI (943556183)

Revised: 3/2024
Document Id: 132a917b-efb9-c0c5-e063-6294a90a12d4
Set id: 677c19eb-780b-479b-ab1d-df249e0af6ea
Version: 15
Effective Time: 20240308
 
United Natural Foods, Inc. dba UNFI