NDC 18027-003 50% Isopropyl Rubbing Alcohol With Wintergreen

Product Information

50% Isopropyl Rubbing Alcohol With Wintergreen is product labeled by American Consumer Products Llc. The product's dosage form is and is administered via form.

Product Code18027-003
Proprietary Name 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.
50% Isopropyl Rubbing Alcohol With Wintergreen
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
American Consumer Products Llc
Labeler Code18027
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for 50% Isopropyl Rubbing Alcohol With Wintergreen?

Product Packages

NDC 18027-003-01

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-02

Package Description: 177 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-03

Package Description: 237 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-04

Package Description: 296 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-05

Package Description: 354 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-06

Package Description: 414 mL in 1 BOTTLE, PLASTIC

NDC 18027-003-07

Package Description: 473 mL in 1 BOTTLE, PLASTIC

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

Product Details

What are 50% Isopropyl Rubbing Alcohol With Wintergreen Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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)
  • PEG-75 LANOLIN (UNII: 09179OX7TB)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

* Please review the disclaimer below.

50% Isopropyl Rubbing Alcohol With Wintergreen Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Otc - Active Ingredient

Active Ingredient (by volume)

Isopropyl alcohol (50% conc.)

Otc - Purpose


Topical Antimicrobial

Indications & Usage


  • decrease germs in minor cuts and scrapes.
  • helps relieve minor muscular aches due to exertion.



For external use only

  • flammable, keep away from fire and flame
  • will produce serious gastric disturbances if taken internally.

Otc - Ask Doctor

Ask a doctor before use if you have deep puncture wounds serious burns

Otc - When Using

When using this product

  • do not get into eyes or mucous membranes
  • use only in a well-ventilated area

Otc - Stop Use

Stop use and ask a doctor if condition persists or gets worse.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of an accidental ingestion, contact a Poison Control Center immediately.

Dosage & Administration


  • apply to skin directly or with clean gauze, cotton or swab
  • for rubbing, apply liberally and rub with hands


Other information

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • keep bottle tightly closed

Inactive Ingredient

Inactive Ingredients

Water (Aqua), Methyl Salicylate, Laneth-75, FD&C Blue #1, FD&C Yellow #5

Package Label.Principal Display Panel



Topical Antimicrobial

12 FL.OZ (354 mL)

* Please review the disclaimer below.