NDC 63843-509 Aloeguard Antimicrobial

  1. Labeler Index
  2. Healthlink
  3. NDC: 63843-509 Aloeguard Antimicrobial

NDC Product Code 63843-509

NDC CODE: 63843-509

Proprietary Name: Aloeguard Antimicrobial 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as antimicrobial

Product Characteristics

Color(s):
GREEN (C48329)

NDC Code Structure

NDC 63843-509-11

Package Description: 208000 mL in 1 DRUM

NDC 63843-509-17

Package Description: 800 mL in 1 BAG

NDC 63843-509-18

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 63843-509-25

Package Description: 532 mL in 1 BOTTLE, PLASTIC

NDC 63843-509-28

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Aloeguard Antimicrobial with NDC 63843-509 is product labeled by Healthlink. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates multiple concept unique identifiers (RXCUI) are associated with this product:


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 LAURYL SULFATE (UNII: 368GB5141J)
  • COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • C9-11 PARETH-6 (UNII: KCE0V8JT7W)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • GLYCOL STEARATE (UNII: 0324G66D0E)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
  • AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Labeler Information

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

Labeler Name: Healthlink
Labeler Code: 63843
Start Marketing Date: 08-20-2013 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: 12-31-2019 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.

Aloeguard Antimicrobial Product Label Images

Aloeguard Antimicrobial 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 Active Ingredient

Chloroxylenol 0.5% w/w

Purpose

Antimicrobial

Keep Out Of Reach Of Children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Uses

 Specially formulated for the sensitive skin of today's healthcare professional


 broad-spectrum antimicrobial hand cleaner


 for repeated washings on a daily basis

Warnings

For external use only When using this product  do not use in or near eyes Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

 wet hands  apply AloeGuard  wash hands vigorously  rinse thoroughly.

Other Information

 store at room temperature

Inactive Ingredients:

Water, Sodium Lauryl Sulfate, Cocamide MIPA, Sodium Laureth Sulfate, Aloe Barbadensis Leaf Juice, Fragrance, C9-11 Pareth-6, Proplyene Glycol, Diazolidinyl Urea, Glycol Stearate, Isopropyl Myristate, Polyquaternium 7, Ammonium Chloride, Methyl Paraben, Propyl Paraben, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazolinone, FD&C Blue #1, FD&C Green #8, D&C Orange #4.

* Please review the disclaimer below.