NDC 81478-001 Popcare

Isopropyl Alcohol

NDC Product Code 81478-001

NDC 81478-001-01

Package Description: 100 CONTAINER in 1 CONTAINER > 2 mL in 1 CONTAINER

NDC 81478-001-02

Package Description: 200 CONTAINER in 1 CONTAINER > 2 mL in 1 CONTAINER

NDC 81478-001-03

Package Description: 80 CONTAINER in 1 BOTTLE > 160 mL in 1 CONTAINER

NDC 81478-001-04

Package Description: 100 BOTTLE in 1 BOTTLE > 200 mL in 1 BOTTLE

NDC 81478-001-05

Package Description: 120 CONTAINER in 1 BOTTLE > 240 mL in 1 CONTAINER

NDC Product Information

Popcare with NDC 81478-001 is a a human over the counter drug product labeled by Ningbo The One Bio-technology Co., Ltd. The generic name of Popcare is isopropyl alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Ningbo The One Bio-technology Co., Ltd

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.

Popcare 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 75 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)

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: Ningbo The One Bio-technology Co., Ltd
Labeler Code: 81478
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: 01-28-2021 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 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’.

* Please review the disclaimer below.

Popcare Product Label Images

Popcare 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(S)

Alcohol 75% Purpose: Antiseptic




Hand sanitizer to help reduce bacteria on the skin.


For external use only. Flammable. Keep away from heat or flame

Otc - When Using

When using the productAvoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.Avoid contact with broken skin.

Otc - Stop Use

Stop use and ask a doctorif irritation or redness develops condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

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


Lift tab at front of the lid to open. Pull up corner of center sheet and thread through dispenser slit in the lid. Pull up exposed wipe and snap off. The next wipe is ready for dispensing.Close lid to retaining moisture. Take wipe and rub thoroughly over all surfaces of both hands. Rub hands briskly together to dry.Dispose of used wipe in trash.Do not Flush.Not recommended for infants

Other Information

Do not store above 105F/40CMay discolor some fabricsHarmful to wooden finishes and plastics

Inactive Ingredients

R0 puter water

* Please review the disclaimer below.