St. Ives Acne Control Apricot Scrub

St. Ives by

Drug Labeling and Warnings

St. Ives by is a Otc medication manufactured, distributed, or labeled by CONOPCO Inc. d/b/a Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB- acne control apricot scrub emulsion 
CONOPCO Inc. d/b/a Unilever

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St. Ives Acne Control Apricot Scrub

ST. IVES ACNE CONTROL APRICOT SCRUB - (salicylic acid) emulsion

St. Ives Acne Control Apricot Scrub

Active ingredient

Salicylic Acid (2%)

Purpose

Acne Treatment

Uses

· For the treatment of acne

Helps prevent new acne pimples and acne blemishes from forming

Warnings

For external use only
When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occues, only use one topical acne medication at a time.
When using this product keep out of eyes. Rinse with water to remove

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Dispense scrub onto fingertips and massage onto damp skin. Spread in small circular motions, then rinse and glow! For best results, use 3-4 times a week

Inactive ingredients

Water (Aqua), Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Glycerin, Cetearyl Alcohol, Zea Mays (Corn) Kernel Meal, Cetyl Alcohol, Triethanolamine, Sodium Lauryl Sulfoacetate, Cocamidopropyl Betaine, Glyceryl Stearate, PEG-100 Stearate, Cetyl Acetate, Benzyl Alcohol, Carbomer, Ceteareth-20, Acetylated Lanolin Alcohol, Polysorbate 60, Fragrance (Parfum), Disodium EDTA, Benzoic Acid, Sorbic Acid, Prunus Armeniaca (Apricot) Fruit Extract, Titanium Dioxide (CI 77891).

Questions or comments?

USA: 1-800-912-9867

Packaging

ST. IVES  BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB
acne control apricot scrub emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1859
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.02 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CORN GRAIN (UNII: C1Z9U7094Z)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
TROLAMINE (UNII: 9O3K93S3TK)
CETYL ALCOHOL (UNII: 936JST6JCN)
PEG-100 STEARATE (UNII: YD01N1999R)
APRICOT (UNII: 269CJD5GZ9)
CETYL ACETATE (UNII: 4Q43814HXS)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYSORBATE 60 (UNII: CAL22UVI4M)
BENZYL ALCOHOL (UNII: LKG8494WBH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
BENZOIC ACID (UNII: 8SKN0B0MIM)
SORBIC ACID (UNII: X045WJ989B)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1859-1	170 g in 1 TUBE; Type 0: Not a Combination Product	02/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	02/15/2021

Labeler - CONOPCO Inc. d/b/a Unilever (001375088)

Revised: 11/2024

Document Id: 2652d303-43fd-9f40-e063-6394a90ad497

34390-5

Set id: bb65b330-cf65-3979-e053-2a95a90a2512

Version: 3

Effective Time: 20241107