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

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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 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. Values = ‘Y’ or ‘N’.

* 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.