ST. IVES BLEMISH CONTROL GREEN TEA 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, Alberto-Culver USA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Salicylic Acid (1%)

PURPOSE

Purpose
Acne Treatment

INDICATIONS & USAGE

Use
For the treatment of acne

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.
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INACTIVE INGREDIENT

Inactive ingredients

Water (Aqua, Eau), Hydrated Silica, Potassium Laureth Phosphate, Glycerin, Sodium Lauroamphoacetate, Sodium Methyl 2-Sulfolaurate, Polyacrylate-1 Crosspolymer, Citric Acid, Glycereth-18 Ethylhexanoate, Disodium 2-Sulfolaurate, Kaolin, Hydrolyzed Jojoba Esters, Fragrance (Parfum), Glycereth-18, Phenethyl Alcohol, PPG-2 Methyl Ether, Olea Europaea (Olive) Leaf Extract, Camellia Sinensis Leaf Extract, Methylisothiazolinone, Yellow 5 (CI 19140), Red 4 (CI 14700), Red 33 (CI 17200), Blue 1 (CI 42090).

QUESTIONS

1-866-912-9867

PRINCIPAL DISPLAY PANEL

PDP

INGREDIENTS AND APPEARANCE

ST. IVES  BLEMISH CONTROL GREEN TEA SCRUB
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1296
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
SODIUM METHYL 2-SULFOLAURATE (UNII: I39GGJ23HV)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y)
DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2)
KAOLIN (UNII: 24H4NWX5CO)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
GLYCERETH-18 (UNII: SA5E43C17C)
PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1296-1	133 mL in 1 TUBE
2	NDC: 64942-1296-2	29 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	06/15/2013

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

Establishment
Name	Address	ID/FEI	Business Operations
Alberto-Culver USA Inc.		021679448	manufacture(64942-1296)