ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB- salicylic acid emulsion

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, Unilever Manufacturing (US), Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Salicylic Acid (2%)

PURPOSE

Purpose
Acne Treatment

INDICATIONS & USAGE

Uses

· For the treatment of acne

· Helps prevent new blackheads and acne blemishes from forming

WARNINGS

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 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.

DOSAGE & ADMINISTRATION

Directions

· Clean the skin thoroughly before applying this product.

· Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily.

· Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if ​​needed or as directed by a doctor.

· If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

INACTIVE INGREDIENT

Inactive ingredients

Water (Aqua), Juglans Regia (Walnut) Shell Powder, Glycol Stearate SE, Glycerin, Sodium Lauryl Sulfoacetate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Prunus Armeniaca (Apricot) Fruit Extract, Cetyl Acetate, Ceteareth-20, Carbomer, Polysorbate 60, Acetylated Lanolin Alcohol, Fragrance (Parfum), PPG-2 Methyl Ether, Phenethyl Alcohol, Methylisothiazolinone, Titanium Dioxide (CI 77891).

QUESTIONS

Questions or comments?
USA: 1-866-912-9867

6 oz PDP

INGREDIENTS AND APPEARANCE

ST. IVES  BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1245
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)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1245-1	283 g in 1 JAR
2	NDC: 64942-1245-2	212 g in 1 TUBE
3	NDC: 64942-1245-3	170 g in 1 TUBE
4	NDC: 64942-1245-4	28 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	03/01/2012

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

Establishment
Name	Address	ID/FEI	Business Operations
Unilever Manufacturing (US), Inc.		021679448	manufacture(64942-1245)