SOFTSAN- alcohol lotion

Kraj: Stany Zjednoczone

Język: angielski

Źródło: NLM (National Library of Medicine)

Składnik aktywny:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Dostępny od:

ABC Compounding Co., Inc.

INN (International Nazwa):

ALCOHOL

Skład:

ALCOHOL 0.7 mL in 1 mL

Droga podania:

TOPICAL

Typ recepty:

OTC DRUG

Wskazania:

Antiseptic for hand-washing to decrease bacteria on the skin, only when water is not available irritation and redness develop

Status autoryzacji:

OTC monograph not final

Charakterystyka produktu

SOFTSAN - ALCOHOL LOTION
ABC COMPOUNDING CO., INC.
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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SOFTSAN 6938 DRUG FACTS AND LABEL
DRUG FACTS BOX OTC-ACTIVE INGREDIENT SECTION
Ethyl Alcohol 62%
DRUG FACTS BOX OTC-PURPOSE SECTION
Antiseptic
DRUG FACTS BOX OTC-INDICATIONS & USAGE SECTION
for hand-washing to decrease bacteria on the skin, only when water is
not available
DRUG FACTS BOX OTC-WARNINGS SECTION
FLAMMABLE, KEEP AWAY FROM FIRE AND FLAMES
FOR EXTERNAL USE ONLY
DRUG FACTS BOX OTC-WHEN USING SECTION
do not get into eyes
if contact occurs, rinse eyes thoroughly with water
DRUG FACTS BOX OTC-STOP USE SECTION
irritation and redness develop
DRUG FACTS BOX OTC-KEEP OUT OF REACH OF CHILDREN SECTION
if swallowed, get medical help or contact a Poison Control Center
right away
DRUG FACTS BOX OTC-DOSAGE & ADMINISTRATION SECTION
wet hands thoroughly with product and allow to dry without wiping
DRUG FACTS BOX OTC-INACTIVE INGREDIENT SECTION
Water, Cetearyl Isononanoate, Ceteareth-20, Cetearyl Alcohol, Glyceryl
Stearate, Glycerin, Ceteareth-
12, Cetyl Palmitate, Carbomer, Diisopropylamine, Sodium Styrene/PEG-10
Maleate/Nonoxynol-10
Maleate/Acrylates Copolymer, Methylparaben, Propylparaben, fragrance,
Tocopheryl Acetate, Aloe
Barbadensis
SOFTSAN 6938 18OZ
693818PA.jpg SoftSan 18oz
SOFTSAN
alcohol lotion
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 2257-9 38
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
0 .7 mL in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
CARBO MER 9 3 4 (UNII: Z135WT9 20 8 )
PRO PYLPARABEN (UNII: Z8 IX2SC1OH)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
.ALPHA.-TO CO PHERO L ACETATE, DL- (UNII: WR1WPI7EW8 )
METHYLPARABEN (UNII: A2I8 C7HI9