FEIX description, usages, side effects, indications, overdosage, supplying and lots more!

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FEIX

SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS

FEIX JABON LIQUIDO FACIAL/ FACIAL LIQUID SOAP




FULL PRESCRIBING INFORMATION

Active ingredient

Feix Facial Liquid soap contains TRICLOSAN, a powerful antibacterial agent. Another one of its components is the active DIPYRITHIONE and BIO-SULFUR used to eliminate Gram positive and Gram negative germs and has a selective action against certain types of fungi.

Purpose

Washing of the face during the dermal infectiuos process of the skin; washing of the skin as a complement for the medical prescription. Please visit your doctor when the dermal process requires a medical diagnosis


Keep this product out of the reach of children


Uses

Facial soap used in persons with oily skin.


Apply an adequate amount on wet skin; create foam rubbing the skin very gently; rinse thoroughly, dry patting softly and seal with Calendula Cream for oily skin.

Contains calendula extract, nettle extract, chamomile extract, and following propierties to improve the condition of the skin: anti-inflamatory, aids in cicatrization, astringent, anti-seborrheic, soothing and also tones the skin.

IMAGE OF THE LABEL

FEIX


FEIX

SULFUR LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:66854-024
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFUR SULFUR 0.2 mL
DIPYRITHIONE 0.5 mL

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
Coco Diethanolamide
GLYCERIN
BUTYLENE GLYCOL
SANGUISORBA OFFICINALIS ROOT
CHINESE CINNAMON
GINGER
GLYCOL DISTEARATE
COCO GLUCOSIDE
GLYCERYL OLEATE
GLYCERYL MONOSTEARATE
propylene glycol
CALENDULA OFFICINALIS FLOWER
CHAMOMILE
URTICA DIOICA LEAF
TRICLOSAN
PEG-120 METHYL GLUCOSE DIOLEATE
TROLAMINE
polysorbate 80
SODIUM CHLORIDE
METHYLPARABEN
CITRIC ACID MONOHYDRATE
PROPYLPARABEN
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:66854-024-01 280 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2012-06-30


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Be sure to consult your doctor before taking any medication!
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