FDA.reportPublic FDA data

Ethyl alcohol

Manufacturer
P & L Development, LLC
Effective date
2019-12-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:55:43

Label at a glance#

ProductEthyl alcohol 70 percent ReadyInCase
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Dosage and administration

clean affected area apply small amount of this product on the area 1-3 times daily if bandaged, let dry first may be covered with a sterile bandage

Label contents#

Full prescribing information#

Active ingredient (by volume)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol (70% conc.)

Purpose

OTC - PURPOSE SECTION

first aid antiseptic

Uses

INDICATIONS & USAGE SECTION

  • first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

For external use only.

  • flammable, keep away from fire or flame
  • if taken internally serious gastric disturbances will result

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture woods, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean affected area
  • apply small amount of this product on the area 1-3 times daily
  • if bandaged, let dry first
  • may be covered with a sterile bandage

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature

Inactive ingredient

INACTIVE INGREDIENT SECTION

acetone, denatonium benzoate, methyl isobutyl ketone, purified water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70% rubbing alcohol

Ethyl

First aid antideptic

Manufactured by:

PL Developments

1874 Hwy 72 W

Clinton, SC 29325

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

WARNING: FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME 

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY FOIL UNDER THE CAP IS BROKEN OR MISSING.

FL OZ (mL

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ReadyInCase 70% Rubbing Alcohol
ReadyInCase 70% Rubbing Alcohol

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
ACETONEINACTIVE INGREDIENT1364PS73AF1
DENATONIUM BENZOATEINACTIVE INGREDIENT4YK5Z54AT21
METHYL ISOBUTYL KETONEINACTIVE INGREDIENTU5T7B88CNP1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49580-027449580-0274-6

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ACETONE1364PS73AFIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
METHYL ISOBUTYL KETONEU5T7B88CNPIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SOLUTION / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2GEL / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
DENATONIUM BENZOATEDENATONIUM BENZOATE4YK5Z54AT2SWAB / TOPICALNAExact identifier — unii candidate
3 equally ranked IID candidates
ACETONEACETONE1364PS73AFTABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c32dd32d-7fa2-45d4-8b2a-dd132956542550f3652e-7783-44c2-a0da-b4a6b2bc00172019-12-04WarningsExact identifier
spl id: c32dd32d-7fa2-45d4-8b2a-dd1329565425
spl set id: 50f3652e-7783-44c2-a0da-b4a6b2bc0017

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.