CLINICIANS COMPLEX- sulfur lotion

Clinicians Complex by

Drug Labeling and Warnings

Clinicians Complex by is a Otc medication manufactured, distributed, or labeled by SkinSx.com, Inc., A.I.G. Technologies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Sulfur 10%

Purpose

Acne Treatment

Uses:

For the treatment of acne Dries up acne pimples Dries and clears acne blemishes

Helps keep skin clear of new acne blemishes

Warnings:

For external use only When using this product 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 Do not use on broken skin or large areas of the skin When using this product apply only to areas with acne.  Avoid contact with eyes If excessive irritation develops or increases, discontinue use and consult a doctor Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions:

​DO NOT SHAKE SOLUTION​  Cleanse the skin thoroughly before applying medication  Dip clean cotton swab into sediment and apply directly to blemishes.  Because excessive drying of the skin may occur, limit use to one application daily, or as directed by a physician.

Inactive Ingredients:

Isopropyl Alcohol, Water, Zinc Oxide, Camphor, Magnesium Aluminum Silicate, Salicylic Acid, Iron Oxides.

Other Information:

Protect this product from excessive heat and direct sun light.

Questions or Comments:

Distibuted by: SkinSx.com, Inc. Buford, GA 30519

770-932-7755 www.skinsx.com Made in USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLINICIANS COMPLEX 
sulfur lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72622-001
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 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
ZINC OXIDE (UNII: SOI2LOH54Z)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
SALICYLIC ACID (UNII: O414PZ4LPZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72622-001-01	31.0 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	11/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/01/2018

Labeler - SkinSx.com, Inc. (077455069)

Establishment
Name	Address	ID/FEI	Business Operations
A.I.G. Technologies, Inc.		171837367	manufacture(72622-001) , label(72622-001)