NDC 41520-170 Antibacterial Foaming Olive And Aloe

  1. Labeler Index
  2. American Sales Company
  3. NDC: 41520-170 Antibacterial Foaming Olive And Aloe

NDC Product Code 41520-170

NDC CODE: 41520-170

Proprietary Name: Antibacterial Foaming Olive And Aloe 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 41520-170-08

Package Description: 236 mL in 1 BOTTLE, PUMP

NDC 41520-170-24

Package Description: 710 mL in 1 BOTTLE

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

NDC Product Information

Antibacterial Foaming Olive And Aloe with NDC 41520-170 is a product labeled by American Sales Company. The generic name of Antibacterial Foaming Olive And Aloe is . The product's dosage form is and is administered via form.

Labeler Name: American Sales Company

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)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • GLYCERETH-26 (UNII: NNE56F2N14)
  • DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • SULISOBENZONE (UNII: 1W6L629B4K)
  • IMIDUREA (UNII: M629807ATL)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
  • PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Labeler Information

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

Labeler Name: American Sales Company
Labeler Code: 41520
Start Marketing Date: 01-21-2011 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: 12-31-2018 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.

Antibacterial Foaming Olive And Aloe Product Label Images

Antibacterial Foaming Olive And Aloe 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

Active Ingredient

TRICLOSAN 0.3 PERCENT

Purpose

ANTISEPTIC

Uses

FOR WASHING TO DECREASE BACTERIA ON THE SKIN.

Warnings

FOR EXTERNAL USE ONLY.

When Using This Product

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.

Stop Using This Product And Ask Doctor If

IRRITATION OR REDNESS DEVELOPS AND LASTS.

Keep Out Of Reach Of Children

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Directions

APPLY ONTO WET HANDS AND WORK INTO A LATHER.  RINSE THOROUGHLY.

Other Information

STORE AT ROOM TEMPERATURE.

Inactive Ingredients

WATER, SODIUM LAURETH SULFATE, GLYCERETH-26, DISODIUM LAURETH
SULFOSUCCINATE, COCAMIDOPROPYL BETAINE, FRAGRANCE, PROPYLENE GLYCOL,
PANTHENOL, ALOE BARBADENSIS LEAF JUICE, XANTHAN GUM, BENZOPHENONE-4,
IMIDAZOLIDYNL UREA, DMDM HYDANTOI N, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-7 GLYCERYL COCOATE, POLYSORBATE
20, TETRASODIUM EDTA, CITRIC ACID, BLUE 1 (CI 42090), YELLOW 10 (CI 47005).

* Please review the disclaimer below.