NDC 62257-369 Clean All
NDC Product Code 62257-369
Proprietary Name: Clean All What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NDC Code Structure
NDC 62257-369-01
Package Description: 1200 mL in 1 CARTRIDGE
NDC 62257-369-03
Package Description: 350 mL in 1 CARTRIDGE
NDC 62257-369-05
Package Description: 540 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-06
Package Description: 1 BAG in 1 BOX > 800 mL in 1 BAG
NDC 62257-369-07
Package Description: 700 mL in 1 BAG
NDC 62257-369-08
Package Description: 1 BAG in 1 BOX > 1000 mL in 1 BAG
NDC 62257-369-09
Package Description: 2000 mL in 1 CARTRIDGE
NDC 62257-369-10
Package Description: 1000 mL in 1 CARTRIDGE
NDC 62257-369-11
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-12
Package Description: 1000 mL in 1 BAG
NDC 62257-369-13
Package Description: 800 mL in 1 BAG
NDC 62257-369-14
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-15
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-16
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-18
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-24
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-27
Package Description: 800 mL in 1 CARTRIDGE
NDC 62257-369-28
Package Description: 149 mL in 1 BOTTLE, PLASTIC
NDC 62257-369-55
Package Description: 208200 mL in 1 DRUM
NDC Product Information
Clean All with NDC 62257-369 is a product labeled by Abc Compounding Co., Inc.. The product's dosage form is and is administered via form.
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: Abc Compounding Co., Inc.
Labeler Code: 62257
Start Marketing Date: 11-01-2010 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.
Clean All Product Label Images
Clean All 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
- Drug Facts Box Otc-Purpose Section
- Drug Facts Box Otc-Indications & Usage Section
- Drug Facts Box Otc-Warnings Section
- Drug Facts Box Otc-When Using Section
- Drug Facts Box Otc-Stop Use Section
- Drug Facts Box Otc-Keep Out Of Reach Of Children Section
- Drug Facts Box Otc-Dosage & Administration Section
- Drug Facts Box Otc-Inactive Ingredient Section
- Clean All 6369 800 Ml
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
Clean All 6369 800 Ml
6369N8PS.jpg Clean All 800 ml
* Please review the disclaimer below.
