NDC 50157-103 Gingerbread

NDC Product Code 50157-103

NDC 50157-103-01

Package Description: 29 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

Gingerbread with NDC 50157-103 is a product labeled by Brands International. The generic name of Gingerbread is . The product's dosage form is and is administered via form.

Labeler Name: Brands International

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)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Brands International
Labeler Code: 50157
Start Marketing Date: 10-01-2015 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: 12-31-2020 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.

Gingerbread Product Label Images

Gingerbread 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

Gingerbread Antibacterial Hand Sanitizer

ACTIVE INGREDIENT: ETHYL ALCOHOL 62%
PURPOSE ANTISEPTIC

Otc - Purpose

ANTISEPTIC

Indications & Usage

USES: TO DECREASE BACTERIA ON THE SKIN AND CLEAN HANDS.
RECOMMENDED FOR REPEATED USE

Warnings

WARNING: FOR EXTERNAL USE ONLY. FLAMMABLE,


KEEP AWAY FROM FIRE OR FLAME.

Otc - When Using

DO NOT GET INTO EYES. IF CONTACT OCCURS,RINSE THROUGHLY WITH WATER.

Otc - Ask Doctor

DISCONTINUE USE IF IRRITATION OR REDNESS DEVELOP. IF IRRITATION PERSISTS FOR MORE THEN 72 HOURS, CONSULT A DOCTOR.

Otc - Keep Out Of Reach Of Children

SUPERVISE CHILDREN IN THE USE OF THIS PRODUCT.

Dosage & Administration

OTHER INFORMATIONMAY DISCOLOR CERTAIN FEBRICS OR SURFACES.

Inactive Ingredient

INACTIVE INGREDIENTS: WATER, ISOPROPYL ALCOHOL, GLYCERIN, CARBOMER, AMINOMETHYL PROPANOL, FRAGRANCE, PROPYLENE GLYCOL, ISOPROPYL MYRISTATE, ALOE BARBADENSIS LEAF JUICE, TOCOPHEROL ACETATE (VITAMIN E), SUNFLOWER (HELIANTHUS ANNUUS) SEED EXTRACT, RED 40 (Cl 16035), Yellow 5 (Cl 19140), Blue 1 (Cl 42090)

* Please review the disclaimer below.