NDC 51384-004 All Clear

NDC Product Code 51384-004

NDC 51384-004-01

Package Description: 500 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

All Clear with NDC 51384-004 is a product labeled by Botanicals Internacional S.a. De C.v.. The generic name of All Clear is . The product's dosage form is and is administered via form.

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

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)

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
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: E - EXPIRED, the listing certification expired. 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.

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.