ST. IVES 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
Treats 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
Wet face.  Apply a generous amount of product over face and neck with fingertips.  Rinse with water.  Use twice daily for best results.  Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water.  Use with Blemish Control Green Tea Gel Cleanser.

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

Salicylic Acid

Hydrolyzed Jojoba Esters

Parfum (Fragrance)

Glycereth-18

Phenethyl Alcohol

PPG-2 Methyl Ether

Epilobium Angustifolium Extract

Olea Europaea (Olive) Leaf Extract

Alteromonas Ferment Extract

Ascophyllum Nodosum Extract

Methylisothiazolinone

Yellow 5 (CI 19140)

CI 14700 (Red 4)

CI 17200 (Red 33)

CI 42090 (Blue 1)

Camellia Sinensis Leaf Extract

Yeast Extract

QUESTIONS

Questions or comments?
Visit us at www.stives.com  1-866-912-9867

PRINCIPAL DISPLAY PANEL

PDP

INGREDIENTS AND APPEARANCE

ST. IVES  GREEN TEA SCRUB
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1247
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 mL  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)
ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
YEAST (UNII: 3NY3SM6B8U)
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: 64942-1247-1	133 mL in 1 TUBE
2	NDC: 64942-1247-2	30 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	03/08/2012

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

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