FEIX BIOAZUFRE / BIOSULPHUR- sulfur soap

FEIX by

Drug Labeling and Warnings

FEIX by is a Otc medication manufactured, distributed, or labeled by SPAI-SONS PHAMACEUTICAL INTERNATIONAL COSMETICS, SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS, SPAI-SONS PHARMACEUTICAL INTERNATIONAL COMSETICS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Feix solid soap, made with coconut fatty esters and sulfur bio-fluid for washing oily skin,or acne-like hyper-secretory.

PURPOSE

Feix solid soap is ideal for washing the skin with rashes, or very sensitive to alkali and soaps made with high concentrations of lye (caustic soda).

KEEP OUT OF REACH OF CHILDREN

This product must be keep out reach of the children.

INDICATIONS & USAGE

This product is indicated for people who have hypersecretion of fat in the skin. It is used as a regular soap bar with the variety that this soap removes impurities from skin oils.

WARNINGS

Feix, does not irritate or dry skin, is well tolerated at any age.

DOSAGE & ADMINISTRATION

Feix biosuphur is topical application, rub the soap on the area to be treated gently massaging foam is generated.

INACTIVE INGREDIENT

This soap is made from a series of the ester type excipients that allow proper formation of soap, besides having ingredients that provide moisture to the skin.

PRINCIPAL DISPLAY PANEL

IMAGE OF THE CARTON LABEL

INGREDIENTS AND APPEARANCE

FEIX  BIOAZUFRE / BIOSULPHUR
sulfur soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66854-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
SODIUM PALMITATE (UNII: JQ43KP6296)
SODIUM STEARATE (UNII: QU7E2XA9TG)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM SARCOSINATE (UNII: 6EHN3PQL8Z)
PARAFFIN (UNII: I9O0E3H2ZE)
SODIUM COCOATE (UNII: R1TQH25F4I)
SODIUM ISETHIONATE (UNII: 3R36J71C17)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERIN (UNII: PDC6A3C0OX)
DIPYRITHIONE (UNII: 9L87N86R9A)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Characteristics
Color	white (BEIGE)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66854-002-01	70 g in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358H	05/01/2006

Labeler - SPAI-SONS PHAMACEUTICAL INTERNATIONAL COSMETICS (880172184)

Registrant - SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)

Establishment
Name	Address	ID/FEI	Business Operations
SPAI-SONS PHARMACEUTICAL INTERNATIONAL COMSETICS		880172184	analysis, label, manufacture, pack