NDC 62651-053 Hand Sanitizer Cinnamon Apple Cider

Alcohol

  1. Labeler Index
  2. Base4 Ventures, Llc.
  3. NDC: 62651-053 Hand Sanitizer Cinnamon Apple Cider

NDC Product Code 62651-053

NDC CODE: 62651-053

Proprietary Name: Hand Sanitizer Cinnamon Apple Cider What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 62651 - Base4 Ventures, Llc.
    • 62651-053 - Hand Sanitizer Cinnamon Apple Cider

NDC 62651-053-01

Package Description: 29.5 mL in 1 BOTTLE

NDC Product Information

Hand Sanitizer Cinnamon Apple Cider with NDC 62651-053 is a a human over the counter drug product labeled by Base4 Ventures, Llc.. The generic name of Hand Sanitizer Cinnamon Apple Cider is alcohol. The product's dosage form is gel and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1039811.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Hand Sanitizer Cinnamon Apple Cider Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

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)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Base4 Ventures, Llc.
Labeler Code: 62651
FDA Application Number: part333E What is the FDA Application Number?
This 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.
Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product 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 www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 01-08-2021 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: 12-31-2022 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: N - NO 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 Cinnamon Apple Cider Product Label Images

Hand Sanitizer Cinnamon Apple Cider 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

Alcohol Denat. 66% (V/V)

Purpose

Antiseptic

Uses

  • Hand sanitizer to help decrease bacteria on the skin.recommended for repeated use.

Warnings

  • For external use only. Flammable. Keep away from heat or flame.Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

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 redness or irritation develop and lasts.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center immediately.

Directions

  • Rub dime sized amount between hands until dry.Supervise children in the use of this product. In the case of eye contact rinse eyes thoroughly with water

Other Information

  • Do not store above 105°F.May discolor some fabrics.

Inactive Ingredients

Water, Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, FD&C Red No. 4, FD&C Yellow No. 5, FD&C Blue No. 1.

* Please review the disclaimer below.