CLIXIT SKIN CARE ACNE DRYING- sulfur acne treatment suspension

Clixit Skin Care Acne Drying by

Drug Labeling and Warnings

Clixit Skin Care Acne Drying by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc., Renu Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Sulfur Colloidal 10%

PURPOSE

Purpose

Acne Treatment

INDICATIONS & USAGE

Use

For treatment of acne. Healing and drying of acne. Penetrates pores to control acne. Helps prevent breakouts.

WARNINGS

Warnings

For external use only

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

Keep out of reach of children.

If swallowed, contact physician or poison control center immediately.

OTHER SAFETY INFORMATION

Store at room temperature

DOSAGE & ADMINISTRATION

Directions

Clean the skin thoroughly before using. Cover affected areas with thin layer two or three times a day

DO NOT USE

Do not use on broken skin or large areas of skin. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

INACTIVE INGREDIENT

Inactive Ingredients

Camphor, Deionized Water, Hippophae Rhamnoides (Seaberry) Fruit and Seed Oil, Iron Oxide, Isopropyl Alcohol, Magnesium Aluminum Silicate, Salicylic Acid, Zinc Oxide.

QUESTIONS

QUESTIONS

Call 844 425 4948

STATEMENT OF IDENTITY

Outer Box

PRINCIPAL DISPLAY PANEL

Drying Lotion Label

INGREDIENTS AND APPEARANCE

CLIXIT SKIN CARE ACNE DRYING 
sulfur acne treatment suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-447
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	2.8 g  in 28 g

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
ZINC OXIDE (UNII: SOI2LOH54Z)
FERRIC OXIDE RED (UNII: 1K09F3G675)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-447-02	1 in 1 BOX	10/02/2019
1	NDC: 76348-447-01	28 g in 1 BOTTLE; 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	10/02/2019

Labeler - Renu Laboratories, Inc. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
Renu Laboratories		945739449	manufacture(76348-447)