NDC 78902-105 Hand Sanitizer Plus Aloe Vera

NDC Product Code 78902-105

NDC 78902-105-02

Package Description: 59 mL in 1 BOTTLE

NDC 78902-105-04

Package Description: 118 mL in 1 BOTTLE

NDC 78902-105-06

Package Description: 177 mL in 1 BOTTLE

NDC 78902-105-08

Package Description: 236 mL in 1 BOTTLE

NDC 78902-105-16

Package Description: 473 mL in 1 BOTTLE

NDC 78902-105-24

Package Description: 739 mL in 1 BOTTLE

NDC 78902-105-32

Package Description: 946 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

Hand Sanitizer Plus Aloe Vera with NDC 78902-105 is product labeled by Jocott Brands, Inc.. 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)
  • POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Product Labeler Information

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

Labeler Name: Jocott Brands, Inc.
Labeler Code: 78902
Start Marketing Date: 07-25-2020 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.

Hand Sanitizer Plus Aloe Vera Product Label Images

Hand Sanitizer Plus Aloe Vera 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

ETHYL ALCOHOL 65%

Purpose

ANTIMICROBIAL

Use

  • HAND SANITIZER CAN HELP REDUCE BACTERIA ON THE SURFACE OF SKIN.

Warnings

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.FOR EXTERNAL USE ONLY.WHEN USING THIS PRODUCT DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.STOP USE AND ASK A DOCTOR IF IRRITATION OR RASH APPEARS AND LASTS.

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

  • APPLY PRODUCT ALL OVER HANDS UNTIL DRY.CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.

Other Information

  • STORE BELOW 110°F (43°C)MAY DISCOLOR CERTAIN FABRICS OR SURFACES

Inactive Ingredients

Purified Water (Aqua), PEG-6, Glycerin, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice, Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum)

* Please review the disclaimer below.