OTC Medication Information: CLEAR CELL Medicated Acne Scrub

CLEAR CELL MEDICATED ACNE SCRUB — benzoyl peroxide cream
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.

Active Ingredient:

Benzoyl Peroxide 3%

Inactive Ingredients:

Water, Cocamidopropyl Hydroxysultane, Micro-Exfoliant Beads, Cera Alba (Bees Wax), Ammonium Laureth Sulfate, Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Extract, Melia Azadirachta (Neem) Leaf Extract, Symphytum Officinale (Comfrey) Extract, Carbomer, Triethanolamine, Mentha Virdis (Spearmint) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Camellia Sinensis (Green Tea) Leaf Extract, Arnica Montana (Arnica) Flower Extract, Chamomilla Recutita (Chamomile) Flower Extract, Aesculus Hippocastanum (Horse Chestnut) Extract, Allantoin, Disodium EDTA.


Other Information on the back of the container:
(Claims)

A micro-exfoliating cleanser with benoyl peroxide to treat active acne. A blend of anti-oxidants soothe irritated and red, inflamed lesions leaving skin healthy and blemish free.
Paraben-free
Directions:
Apply a liberal amount to wet face and massage for 1 minute. This gentle exfoliation process assists in reducing active acne and thoroughly cleansing oily skin. Rinse with cold water. Use morning and evening. Note: Do not overstimulate active lesions.
Indications:
Active acne and acne-prone skin.

Distributor:
Image International

Palm Beach, FL 33411 USA

www.imageskincare.com

Image of the Product:

CLEAR CELL Medicated Acne Scrub:

Image of the Product
(click image for full-size original)
CLEAR CELL MEDICATED ACNE SCRUB
benzoyl peroxide cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4034
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZOYL PEROXIDE (BENZOYL PEROXIDE) BENZOYL PEROXIDE 30 mg in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62742-4034-1 177.6 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.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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