CLIXIT ACNE DRYING- sulfur lotion

CLIXIT ACNE DRYING by

Drug Labeling and Warnings

CLIXIT ACNE DRYING by is a Otc medication manufactured, distributed, or labeled by Clixit, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredient

Sulfur 10%

Purpose

Acne Treatment

Use:

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

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.Stop use and ask a doctor if skin irritation occurs or gets worse. Rinse right away with water if product gets in eyes.

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

Directions:

DO NOT SHAKE BOTTLE.
Clean the skin thoroughly before using at night. Apply only to areas with acne. Allow solution to dry and rinse off in the morning.

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

Inactive Ingredients:

Allantoin, Aqua (Deionized Water), Camphor, Ethylhexylglycerin, Iron Oxide, Isopropyl Alcohol, Magnesium Aluminium Silicate, Phenoxyethanol, Salicylic Acid, Zinc Oxide.

SPL UNCLASSIFIED SECTION

Overnight Treatment

For stubborn acne

SKINCARE BY CLIXIT®

POWERFUL SULFUR AND SALICYLIC ACID FORMULA penetrates pores and dries out stubborn acne overnight revealing smaller, less noticeable blemishes.

Clears acne and allows skin to heal

Emergency spot treatment

Reduces size of stubborn acne

Results overnight

Ideal for all skin types

POWERFUL OVERNIGHT ACNE TREATMENT

QUESTIONS?
Call 844-425-4948

Made in the USA

Distributed by
Clixit, LLC, Orlando, FL

NOT TESTED ON ANIMALS

Packaging

INGREDIENTS AND APPEARANCE

CLIXIT ACNE DRYING 
sulfur lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71328-042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FERRIC OXIDE RED (UNII: 1K09F3G675)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SALICYLIC ACID (UNII: O414PZ4LPZ)
ZINC OXIDE (UNII: SOI2LOH54Z)

Product Characteristics
Color	pink	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71328-042-02	1 in 1 BOX	02/01/2021
1	NDC: 71328-042-01	29 mL 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	02/01/2021

Labeler - Clixit, Llc (014971694)