Clear Cell Cleanser: Package Insert and Label Information

CLEAR CELL CLEANSER — salicylic acid gel
Allure Labs, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

INDICATIONS AND USAGE SECTION:

A daily Salicylic acid cleanser that exfoiates, gently removes makeup and diminishes excess oil. Anti-oxidants keep skin soft, purified and shine-free.

Paraben free

DIRECTIONS:

Apply to wet face and massage for 1 minute. Repeat cleansing for additional exfoliation.

INDICATIONS:

Acne and acne-prone skin

ACTIVE INGREDIENTS:

Salicylic Acid

INACTIVE INGREDIENTS:

Water (Aqua), Ammonium Laureth Sulfate, Disodium cocoamphodiacetate, Glycerin, PEG 120 Methyl Glucose Dioleate, Phenoxyethanol, Caprylyl Glycol, Camellia sinensis (Green Tea) leaf extract, Ethylhexylglycerin, Polyquaternium-10, Hexylene Glycol, Arnica montana (Arnica) flower extract, Chamomilla recutita (Chamomile) flower extract, Aesculus hippocastanum (Horse Chestnut) extract, Melia azadirachta (neem) leaft extract, Hamamelis virginiana (Witch Hazel) water, Melaleuca alternifolia (Tea Tree) leaf oil, Mentha viridis (spearmint) oil, Eucalyptus globulus (Eucalyptus) leaf oil.

DISTRIBUTOR:

Image International

Palm Beach, FL 33411 USA


IMAGE OF PRINCIPAL DISPLAY PANEL:
Image of Product: Clear Cell Salicylic Gel Cleanser
(click image for full-size original)

Image of Product: Clear Cell Salicylic Gel Cleanser
CLEAR CELL CLEANSER
salicylic acid gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4045
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 30 mg in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62742-4045-1 177.6 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333 01/01/2010
Labeler — Allure Labs, Inc. (926831603)

Revised: 07/2010 Allure Labs, Inc.

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.