NDC 76016-544 Pure Kleen

NDC Product Code 76016-544

NDC 76016-544-01

Package Description: 1200 mL in 1 CARTRIDGE

NDC 76016-544-03

Package Description: 350 mL in 1 CARTRIDGE

NDC 76016-544-05

Package Description: 540 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-06

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

NDC 76016-544-07

Package Description: 700 mL in 1 BAG

NDC 76016-544-08

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

NDC 76016-544-09

Package Description: 2000 mL in 1 CARTRIDGE

NDC 76016-544-10

Package Description: 1000 mL in 1 CARTRIDGE

NDC 76016-544-11

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-12

Package Description: 1000 mL in 1 BAG

NDC 76016-544-13

Package Description: 800 mL in 1 BAG

NDC 76016-544-14

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-15

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-16

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-17

Package Description: 532 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-18

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-19

Package Description: 18900 mL in 1 CONTAINER

NDC 76016-544-20

Package Description: 75600 mL in 1 DRUM

NDC 76016-544-24

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-27

Package Description: 800 mL in 1 CARTRIDGE

NDC 76016-544-28

Package Description: 149 mL in 1 BOTTLE, PLASTIC

NDC 76016-544-35

Package Description: 132500 mL in 1 DRUM

NDC 76016-544-55

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

Pure Kleen with NDC 76016-544 is a product labeled by Arrow-magnolia International, Inc,. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 413261.

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)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Labeler Information

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

Labeler Name: Arrow-magnolia International, Inc,
Labeler Code: 76016
Start Marketing Date: 01-01-2011 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: 12-31-2017 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.

Pure Kleen Product Label Images

Pure Kleen 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

Chloroxylenol 0.3%

Drug Facts Box Otc-Purpose Section

Antiseptic

Drug Facts Box Otc-Indications & Usage Section

For hand-washing to decrease bacteria on the skin

Drug Facts Box Otc-Warnings Section

For 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

  • Wet hands and forearmsapply 5 milliliters (teaspoonful) or palmful to hands and forearms scrub thoroughly for 1 minute and rinse

Drug Facts Box Otc-Inactive Ingredient Section

Water, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, sodium chloride, citric acid, fragrance, FD and C yellow no.5, food red 10

Pure Kleen 6544 1 Gal

6544F1S6046.jpg  Pure Kleen  1 gal

* Please review the disclaimer below.