NDC 82167-000 Tinfu Isopropyl Alcohol Prep Pads

Isopropyl Alcohol

NDC Product Code 82167-000

NDC 82167-000-01

Package Description: .12 mL in 1 PATCH

NDC 82167-000-02

Package Description: 100 PACKET in 1 BOX > .12 mL in 1 PACKET

NDC 82167-000-03

Package Description: 200 PACKET in 1 BOX > .12 mL in 1 PACKET

NDC 82167-000-04

Package Description: 300 PACKET in 1 BOX > .12 mL in 1 PACKET

NDC 82167-000-05

Package Description: .25 mL in 1 PATCH

NDC 82167-000-06

Package Description: 100 PACKET in 1 BOX > .25 mL in 1 PACKET

NDC 82167-000-07

Package Description: 200 PACKET in 1 BOX > .25 mL in 1 PACKET

NDC 82167-000-08

Package Description: 300 PACKET in 1 BOX > .25 mL in 1 PACKET

NDC 82167-000-09

Package Description: .56 mL in 1 PATCH

NDC 82167-000-10

Package Description: 100 PACKET in 1 BOX > .56 mL in 1 PACKET

NDC 82167-000-11

Package Description: 200 PACKET in 1 BOX > .56 mL in 1 PACKET

NDC 82167-000-12

Package Description: 300 PACKET in 1 BOX > .56 mL in 1 PACKET

NDC Product Information

Tinfu Isopropyl Alcohol Prep Pads with NDC 82167-000 is a a human over the counter drug product labeled by Shandong T&f Nonwoven Co., Ltd. The generic name of Tinfu Isopropyl Alcohol Prep Pads is isopropyl alcohol. The product's dosage form is cloth and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 797544.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

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.

Tinfu Isopropyl Alcohol Prep Pads 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.

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: Shandong T&f Nonwoven Co., Ltd
Labeler Code: 82167
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: 08-25-2021 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.

Tinfu Isopropyl Alcohol Prep Pads Product Label Images

Tinfu Isopropyl Alcohol Prep Pads 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


  • This is a hand sanitizer manufactured according to the
  • Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
  • The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.Glycerol (1.45% v/v).Hydrogen peroxide (0.125% v/v).Sterile distilled water or boiled cold water.The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(S)

Isopropyl Alcohol, 70% v/v




For preparation of the skin prior to injection.


For external use only. Flammable,keep away from fire or flame.

Do Not Use

  • With electrocautery procedures.

Otc - When Using

When using this product do not get into eyes. do not apply over large areas of the body. in case of deep or puncture wounds, animal bites or serious burns, consult a doctor. use only in a well ventilated area.

Otc - Stop Use

Stop use and ask a doctor if irritation and redness develops.

Females & Males Of Reproductive Potential

If pregnant or breastfeeding ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center right away.


  • Apply to skin as needed.Discard after single use.

Other Information

  • Store at room temperature 15-30C (59-86F)

Inactive Ingredients


* Please review the disclaimer below.