Medication Guide App

Sani-Silk

Dosage form: lotion
Ingredients: ALCOHOL 0.7mL in 1mL
Labeler: ABC Compounding Co., Inc.
NDC Code: 62257-365

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.

Sani-Silk 6605 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

Sani-Silk 6365 18oz

636518PS.jpg  Sani-Silk  18oz 

SANI-SILK 
alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-365
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CARBOMER 934 
PROPYLPARABEN 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
METHYLPARABEN 
DIISOPROPYLAMINE 
CETEARYL ISONONANOATE 
CETEARETH-12 
CETOSTEARYL ALCOHOL 
GLYCERYL MONOSTEARATE 
CETYL PALMITATE 
Packaging
#Item CodePackage Description
1NDC:62257-365-061 BAG (BAG) in 1 BOX
1800 mL in 1 BAG
2NDC:62257-365-17532 mL in 1 BOTTLE, PLASTIC
3NDC:62257-365-24118 mL in 1 BOTTLE, PLASTIC
4NDC:62257-365-011200 mL in 1 CARTRIDGE
5NDC:62257-365-03350 mL in 1 CARTRIDGE
6NDC:62257-365-05540 mL in 1 BOTTLE, PLASTIC
7NDC:62257-365-07700 mL in 1 BAG
8NDC:62257-365-092000 mL in 1 CARTRIDGE
9NDC:62257-365-101000 mL in 1 CARTRIDGE
10NDC:62257-365-111000 mL in 1 BOTTLE, PLASTIC
11NDC:62257-365-121000 mL in 1 BAG
12NDC:62257-365-13800 mL in 1 BAG
13NDC:62257-365-143785 mL in 1 BOTTLE, PLASTIC
14NDC:62257-365-15946 mL in 1 BOTTLE, PLASTIC
15NDC:62257-365-28149 mL in 1 BOTTLE, PLASTIC
16NDC:62257-365-27800 mL in 1 CARTRIDGE
17NDC:62257-365-55208200 mL in 1 DRUM
18NDC:62257-365-081 BAG (BAG) in 1 BOX
181000 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/01/2010
Labeler - ABC Compounding Co., Inc. (003284353)
Establishment
NameAddressID/FEIOperations
ABC Compounding Co., Inc.003284353manufacture

Revised: 12/2010
 
ABC Compounding Co., Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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