NDC 51384-004 All Clear

Hand Sanitizer- Alcohol Gel

NDC Product Code 51384-004

NDC 51384-004-01

Package Description: 500 mL in 1 BOTTLE

NDC Product Information

All Clear with NDC 51384-004 is a a human over the counter drug product labeled by Botanicals Internacional S.a. De C.v.. The generic name of All Clear is hand sanitizer- alcohol gel. The product's dosage form is gel and is administered via topical form.

Labeler Name: Botanicals Internacional S.a. De C.v.

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.

All Clear 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.

  • ALCOHOL 70 mL/100mL

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.

  • ACRYLIC ACID (UNII: J94PBK7X8S)
  • WATER (UNII: 059QF0KO0R)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERIN (UNII: PDC6A3C0OX)

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.
  • 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: Botanicals Internacional S.a. De C.v.
Labeler Code: 51384
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: 07-07-2020 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: 12-31-2021 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 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.

All Clear Product Label Images

All Clear 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 70%

Purpose

Antimicrobial

Warnings

  • WarningsFor External use only FlammableKeep away from fire or flame

Stop Use

  • Stop use and ask doctorIf irritation and redness persist for more then 72 hours.

Keep Out Of Reach

Keep out of reach of childrenIn case of accidental ingestion, seek medicalattention or contact a poison control center immediately

Uses

  • Hand sanitizer to decrease bacteria on the skinRecommended for repeated use

Directions

  • DIRECTIONSPlace enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.Children under six years of age should be supervised when using this product.

Storage

  • Other InformationStore at 1°C - 30°C (34 °F - 86 °F)

Inactive Ingredients

  • Inactive IngredientsCarbomer, Glycerin, Triethanolamine, Water

Administration

  • Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.Children under six years of age should be supervised when using this product.

Pdp

500MLNDC: 51384-004-01NDC SOURCE: 77070-700-80

* Please review the disclaimer below.