NDC 71012-111 Activeclean

NDC Product Code 71012-111

NDC CODE: 71012-111

Proprietary Name: Activeclean 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.

Product Characteristics

Color(s):
WHITE (C48325)

NDC Code Structure

  • 71012 - Cleanspot, Inc.

NDC 71012-111-60

Package Description: 1 BOTTLE, SPRAY in 1 CONTAINER > 3 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Activeclean with NDC 71012-111 is a product labeled by Cleanspot, Inc.. The product's dosage form is and is administered via form.

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)
  • .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
  • APRICOT SEED OIL (UNII: 54JB35T06A)
  • LEMON OIL (UNII: I9GRO824LL)
  • PEPPERMINT OIL (UNII: AV092KU4JH)

Product Labeler Information

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

Labeler Name: Cleanspot, Inc.
Labeler Code: 71012
Start Marketing Date: 12-01-2016 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: 12-31-2017 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.

Activeclean Product Label Images

Activeclean 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

Dosage & Administration

Shake container. Use enough product to throughly cover hands. Rub hands together briskly until dry. Children under 6 use only with adult supervision.

Warnings

For External Use only. Flammable. Keep away from fire or flame.When using the product, do not use it in or near the eyes. In case of contact, rinse eyes throughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. If swallowed get medical help or contact a PoisonControl Center right away.

Inactive Ingredient

Water, isopropyl alcohol (rubbing alcohol), beeswax, apricit seed oil, tocopherol (Vitamin E), essential oils of lemon and peppermint,(epsilon) - polylysine

Otc - Purpose

Antimicrobial

Otc - Active Ingredient

Ethanol 62% v/v

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Indications & Usage

  • Hand sanitizer to help reduce bacteria on skin that could cause diseaseRecommended for repeated use

* Please review the disclaimer below.