NDC 51263-3125 Vanilla Hand Sanitizer

NDC Product Code 51263-3125

NDC 51263-3125-2

Package Description: 59 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

Vanilla Hand Sanitizer with NDC 51263-3125 is a product labeled by Mgs Group Limited. The generic name of Vanilla Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Mgs Group Limited

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Mgs Group Limited
Labeler Code: 51263
Start Marketing Date: 06-18-2012 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Vanilla Hand Sanitizer Product Label Images

Vanilla 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

Active Ingredient

Ethyl Alcohol 62%

Purpose

Sanitizer

Uses

  • To decrease bacteria on the skin that could cause diseaserecommended for repeated use

Warnings

For external use only- hands.Use only as directedExcessive use or prolonged exposure may cause irritation to skin.Discontinue use if rash, redness or itching occurs.Flammable. Keep away from heat and flame.

When Using This Product

  • Keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor.avoid contact with broken skin.

Stop Use And Ask A Doctor If

Irritation or redness develops

Keep Out Of Reach Of Children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Put a thumb size amount in your palm and rub hands together briskly until dry.

Other Information

  • Do not store in temperatures over 118FChildren under 6 years of age should be supervised while using this productmay discolor certain fabrics

Inactive Ingredients

Aloe barbadensis gel, carbomer, fragrance, glycerin, propylene glycol, tocopherol, triethanolamine, water.

Product Labeling

Vanilla Hand Sanitizernet 2 fl oz (59mL)Drug Facts InsideHand Sanitizer - VanillaManufactured for MGSMGS Group, Ltd.2012 MGS Group, Ltd2229 Barry AvenueLos Angeles, CA 90064Made in China

* Please review the disclaimer below.