CLIXIT TINTED BLEMISH CONCEALER LIGHT SHADE- sulfur acne treatment cream

CLIXIT Tinted Blemish Concealer Light Shade by

Drug Labeling and Warnings

CLIXIT Tinted Blemish Concealer Light Shade by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Sulfur 4%

PURPOSE

Purpose

Acne Treatment

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately.

QUESTIONS

QUESTIONS?

Call 844 425 4948

WARNINGS

Warnings:

For external use only.

Using other topical acne medications at the same time may increase dryness or irritation of the skin.

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 doctor. If bothersome dryness or peeling occurs, reduce application to once per day.

Use For:

For the treatment of acne.

DOSAGE & ADMINISTRATION

Directions:

Clean the skin thoroughly before using. Cover entire affected area. Do not use on broken skin or large areas of the skin. For best results use 2-3 times per day.

Other Ingredients:

Bentonite, Cannabis Sativa (Hemp) Seed Oil, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Deionized Water, Euphorbia Cerifera (Candelilla) Wax, Glycerol Monostearate, Hippophae Rhamnoides (SeaBerry) Fruit and Seed Oil, Iron Oxide, Phenoxyethanol, Steareth-20, Titanium Dioxide, Zinc Oxide.

STATEMENT OF IDENTITY

TINTED BLEMISH CONCEALER

LIGHT SHADE

PRINCIPAL DISPLAY PANEL

TINTED BLEMISH CONCEALER TUBE

CLIXIT TintedBlemishConcealer LIGHT

INGREDIENTS AND APPEARANCE

CLIXIT TINTED BLEMISH CONCEALER LIGHT SHADE 
sulfur acne treatment cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-442
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	0.56 g  in 14 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENTONITE (UNII: A3N5ZCN45C)
ZINC OXIDE (UNII: SOI2LOH54Z)
CORN OIL (UNII: 8470G57WFM)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
CANDELILLA WAX (UNII: WL0328HX19)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-442-02	1 in 1 BOX	09/23/2019
1	NDC: 76348-442-01	14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/23/2019

Labeler - Renu Laboratories, Inc. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories, Inc.		945739449	manufacture(76348-442)