NDC 81754-010 Provtect Hand Sanitizer

Chlorine Dioxide

NDC Product Code 81754-010

NDC 81754-010-01

Package Description: 500 mL in 1 BOTTLE, SPRAY

NDC Product Information

Provtect Hand Sanitizer with NDC 81754-010 is a a human over the counter drug product labeled by Ignal. The generic name of Provtect Hand Sanitizer is chlorine dioxide. The product's dosage form is spray and is administered via topical form.

Labeler Name: Ignal

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Provtect Hand Sanitizer 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.

  • CHLORINE DIOXIDE .05 g/500mL

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)

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: Ignal
Labeler Code: 81754
Marketing Category: UNAPPROVED DRUG OTHER - 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: 04-01-2021 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.

Provtect Hand Sanitizer Product Label Images

Provtect Hand Sanitizer 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

Chlorine Dioxide 0.01%

Inactive Ingredient





For external use only. Avoid direct sunlight and store in a cool place.--------------------------------------------------------------------------------------------------------Do not use• in children less than 2 months of age• internal wound • inhalation by fumigation--------------------------------------------------------------------------------------------------------When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.--------------------------------------------------------------------------------------------------------Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.--------------------------------------------------------------------------------------------------------Keep out of reach of children. If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.

Keep Out Of Reach Of Children

If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.


■ Hand Sanitizer help to reduce germs and inactivate viruses that potentially can cause disease.


■ Spray on or Wet palms, rub hands thoroughly together until dry.■ Supervise children under 6.

Other Information

■ Store between 5-20C (41-68F)■ Avoid freezing and excessive heat above 40C (104F)


Questions [email protected]

* Please review the disclaimer below.