ST. IVES- salicylic acid emulsion

ST. IVES by

Drug Labeling and Warnings

ST. IVES by is a Otc medication manufactured, distributed, or labeled by Cosmetic Laboratories of America. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Use

Treats Acne

Warnings

For external use only.

Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one product should be used unless directed by a doctor.

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

Directions

Pour onto moistened pouf, sponge or hands. Work into a rich, creamy lather and rinse. Avoid contact with eyes. In case of contact with eyes flush thoroughly with water

Inactive Ingredients

Water, Sodium Laureth Sulfate, Bentonite, Cocamidopropyl Betaine, Acrylates Copolymer, Epilobium Angustifolium Extract, Olea Europaea (Olive) Leaf Extract, Ascophyllum Nodosum Extract, Alteromonas Ferment Extract, Yeast Extract, Camellia Sinensis Leaf Extract, Sodium Hydroxide, Glycerin, Disodium EDTA, Polyquaternium-7, Phenethyl Alcohol, PPG-2 Methyl Ether, Methylisothiazolinone, Fragrance, Green 5, Yellow 10, Yellow 5, Red 4, Red 33, Blue 1.

Questions?

1-866-912-9867

PRINCIPAL DISPLAY PANEL - 266 mL Bottle Label

NEW!

St. Ives®

NATURALLY CLEAR

BODY SCRUB
GREEN TEA

CLEARS BODY BREAKOUTS
& REDUCES REDNESS

OIL-FREE
salicylic acid acne medication
with 100% natural green tea

9 fl oz | 266ml

INGREDIENTS AND APPEARANCE

ST. IVES   BODY SCRUB NATURALLY CLEAR SKIN GREEN TEA
salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54726-0500
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 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Laureth Sulfate (UNII: BPV390UAP0)
Bentonite (UNII: A3N5ZCN45C)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Sodium Hydroxide (UNII: 55X04QC32I)
Glycerin (UNII: PDC6A3C0OX)
Edetate Disodium (UNII: 7FLD91C86K)
Phenylethyl Alcohol (UNII: ML9LGA7468)
Olea Europaea Leaf (UNII: MJ95C3OH47)
Ascophyllum Nodosum (UNII: 168S4EO8YJ)
Methylisothiazolinone (UNII: 229D0E1QFA)
D&C Green No. 5 (UNII: 8J6RDU8L9X)
D&C Yellow No. 10 (UNII: 35SW5USQ3G)
Yeast (UNII: 3NY3SM6B8U)
Green Tea Leaf (UNII: W2ZU1RY8B0)
Fd&C Yellow No. 5 (UNII: I753WB2F1M)
Fd&C Red No. 4 (UNII: X3W0AM1JLX)
Fd&C Blue No. 1 (UNII: H3R47K3TBD)
D&C Red No. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54726-0500-9	266 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	02/14/2011

Labeler - Cosmetic Laboratories of America (617165329)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmetic Laboratories of America		617165329	ANALYSIS, MANUFACTURE