NDC 51263-3183 Sweet Berry Hand Sanitizer

NDC Product Code 51263-3183

NDC 51263-3183-2

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

Sweet Berry Hand Sanitizer with NDC 51263-3183 is a product labeled by Mgs Group Limited. The generic name of Sweet Berry 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.

  • WATER (UNII: 059QF0KO0R)
  • .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE (UNII: V5VD430YW9)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CARBOMER 934 (UNII: Z135WT9208)
  • TROLAMINE (UNII: 9O3K93S3TK)

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: 10-17-2012 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: 12-31-2018 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Sweet Berry Hand Sanitizer Product Label Images

Sweet Berry 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

Otc - Active Ingredient

Active Ingredient                                             PurposeEthyl Alcohol         62%             **********        Antiseptic

Otc - Purpose

Hand sanitizer to help decrease bacteria on the skin. when water, soap and towel are not available.Recommended for repeat use

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

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

Warnings

For external use only.Flammable, keep away from fire or flame.Do not apply around eyes; Do not use in ears and mouth.When using this products, avoid contact with eyes. In case of contact, flush eyes with water.Stop use and ask a doctor, if redness or irritation develop and persist for more than 72 hours.Do not store in temperatures over 118°FChildren under 6 years of age should be supervised while using this products.May discolor certain fabrics.

Dosage & Administration

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

Inactive Ingredient

Water, Triethanolamine, Glycerin, Propylene glycol, Tocopheryl, Aloe Barbadensis gel, Carbomer, Fragrance

* Please review the disclaimer below.