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Drug Information

Product NDC: 20276-150

Proprietary Name: Lucky Instant Hand Sanitizer with Vitamin E and Moisturizers

Non Proprietary Name: Ethyl Alcohol

Active Ingredient(s):
  • 62 mL/100mL ALCOHOL

Administration Route(s): TOPICAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Delta Brands Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Start Marketing Date:3/1/2010

Package Information

No. Package Code Package Description Billing Unit
120276-150-022 BOTTLE, SPRAY in 1 BLISTER PACK (20276-150-02) / 60 mL in 1 BOTTLE, SPRAY (20276-150-01)
220276-150-05148 mL in 1 BOTTLE, PUMP (20276-150-05)
320276-150-08237 mL in 1 BOTTLE, PUMP (20276-150-08)
420276-150-10296 mL in 1 BOTTLE, PUMP (20276-150-10)
520276-150-12355 mL in 1 BOTTLE, PUMP (20276-150-12)
620276-150-24710 mL in 1 BOTTLE, PUMP (20276-150-24)
720276-150-361065 mL in 1 BOTTLE, PUMP (20276-150-36)
820276-150-401183 mL in 1 BOTTLE, PUMP (20276-150-40)
920276-150-481420 mL in 1 BOTTLE, PUMP (20276-150-48)
1020276-150-6060 mL in 1 BOTTLE, SPRAY (20276-150-60)
1120276-150-641893 mL in 1 BOTTLE, PLASTIC (20276-150-64)
1220276-150-75222 mL in 1 BOTTLE, PUMP (20276-150-75)
1320276-150-853785 mL in 1 BOTTLE, PLASTIC (20276-150-85)

NDC Record

Field Name Field Value Definition
PRODUCT NDC20276-150The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELucky Instant Hand Sanitizer with Vitamin E and MoisturizersThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEthyl AlcoholThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at under Structured Product Labeling Resources.
APPLICATION NUMBERpart333EThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEDelta Brands IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALCOHOLAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

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This page was last updated on: 2/1/2023