NDC 68654-585 Foamahol

NDC Product Code 68654-585

NDC 68654-585-01

Package Description: 1200 mL in 1 CARTRIDGE

NDC 68654-585-03

Package Description: 350 mL in 1 CARTRIDGE

NDC 68654-585-05

Package Description: 540 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-06

Package Description: 1 BAG in 1 BOX > 800 mL in 1 BAG

NDC 68654-585-07

Package Description: 700 mL in 1 BAG

NDC 68654-585-08

Package Description: 1 BAG in 1 BOX > 1000 mL in 1 BAG

NDC 68654-585-09

Package Description: 2000 mL in 1 CARTRIDGE

NDC 68654-585-10

Package Description: 1000 mL in 1 CARTRIDGE

NDC 68654-585-11

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-12

Package Description: 1000 mL in 1 BAG

NDC 68654-585-13

Package Description: 800 mL in 1 BAG

NDC 68654-585-14

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-15

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-16

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-17

Package Description: 532 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-18

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-24

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-27

Package Description: 800 mL in 1 CARTRIDGE

NDC 68654-585-28

Package Description: 149 mL in 1 BOTTLE, PLASTIC

NDC 68654-585-55

Package Description: 208200 mL in 1 DRUM

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Foamahol with NDC 68654-585 is a product labeled by Share Corporation. The generic name of Foamahol is . The product's dosage form is and is administered via form.

Labeler Name: Share Corporation

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Share Corporation
Labeler Code: 68654
Start Marketing Date: 09-01-2009 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Foamahol Product Label Images

Foamahol Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

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 flamesFor external use only

Drug Facts Box Otc-When Using Section

Do not get into eyesif 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

Press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your handrub hands together and allow to dry without wiping

Drug Facts Box Otc-Inactive Ingredient Section

Water, DEA-C8-18 perfluoroalkylethyl phosphate, propylene glycol, fragrance

Foamahol 6585 18Oz

658518P4292.jpg Foamahol 18oz

* Please review the disclaimer below.