NDC 69898-501 Premium Hand Sanitizer

NDC Product Code 69898-501

NDC 69898-501-01

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 69898-501-07

Package Description: 221 mL in 1 BOTTLE, PLASTIC

NDC 69898-501-08

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC 69898-501-12

Package Description: 354 mL in 1 BOTTLE, PLASTIC

NDC 69898-501-32

Package Description: 946 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

Premium Hand Sanitizer with NDC 69898-501 is product labeled by Md Science Lab Llc. 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 a single concept unique identifier (RXCUI) is 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)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)

Product Labeler Information

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

Labeler Name: Md Science Lab Llc
Labeler Code: 69898
Start Marketing Date: 04-05-2020 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: 12-31-2021 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.

Premium Hand Sanitizer Product Label Images

Premium Hand Sanitizer 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

Other

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

  • For hand sanitizing to decrease bacteria on the skinRecommended for repeated use

Warnings

  • For external use only.

Otc - When Using

  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Otc - Stop Use

  • Stop use and a ask doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Pump a small amount of liquid into palm of hand.Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry.

Inactive Ingredients

Water (aqua), Propylene Glycol, Polysorbate 20, Phenoxyethanol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Aloe barbadensis (Aloe Vera).

* Please review the disclaimer below.