NDC 78658-001 Champ


NDC Product Code 78658-001

NDC 78658-001-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-02

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-03

Package Description: 104 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-04

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-05

Package Description: 177 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-06

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-07

Package Description: 296 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-08

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-09

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-10

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-11

Package Description: 208198 mL in 1 BOTTLE, PLASTIC

NDC 78658-001-12

Package Description: 1040990 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Champ with NDC 78658-001 is a a human over the counter drug product labeled by Champ Products, Ltd. The generic name of Champ is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Champ Products, Ltd

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.

Champ 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.

  • WATER (UNII: 059QF0KO0R)
  • GUARAPROLOSE (3500 MPA.S AT 1%) (UNII: 3A1I7376TC)

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: Champ Products, Ltd
Labeler Code: 78658
FDA Application Number: part333A 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: 05-24-2020 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’.

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Champ Product Label Images

Champ 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%




Hand Sanitizer to help reduce bacteria that potentially can cause disease.


Apply liberally to front and back of hands. Allow to dry. Recommended for repeated use.


For external use only: hands.Flammable, keep away from fire or flame.When using this product avoid contact with the eyes. In case of contact, Rinse eyes thoroughly with water.Stop use and ask a doctor if irritation or redness appears and lasts.If swallowed, get medical help or contact a Poison Control Center immediately.Do not use: in children less than 2 months of age and on open wounds. Do not inhale or ingest.Supervise children under 6 years of age when using the product to avoid swallowing.Other informationStore between 00C (320F) – 410C (1050F)

Inactive Ingredients

Glycerin, Hydrogen Peroxide, Distilled Water, Polymer, Fragrance.Customer service1-833-SANITIZE

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