Hollywood Cosmetics 70% Ethyl Alcohol

Manufacturer
Hollywood Cosmetics, LLC
Effective date
2020-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:16

Label at a glance#

ProductHollywood Cosmetics 70% Ethyl Alcohol
Active ingredientALCOHOL
Label structure12 sections

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

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

If taken internally, serious gastric disturbances will result

Flammable, keep away from fire or flame

Use only in a well-ventilated area, fumes may be toxic

OTC - WHEN USING SECTION

When using this product:

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center right away (800-222-1222)

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

STORAGE AND HANDLING SECTION

  • Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.

OTC - STOP USE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

473 mL NDC: 74223-700-16 16 Oz First Aid Antiseptic (70%)16 Oz First Aid Antiseptic (70%)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74223-700-162022-01-28C16284748780-1d6a99b39-e447-a426-e053-dadaa90af4c2b11abfc2-ac84-fd1f-e053-2a95a90ad34a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74223-700-16Hollywood Cosmetics 70% Ethyl Alcohol473 mL in 1 BOTTLELIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74223-700HOLLYWOOD COSMETICS 70% ETHYL ALCOHOL (ALCOHOL) LIQUID [HOLLYWOOD COSMETICS, LLC]1Legacy NDC, 1 package rows20201009_b11abfc2-ac84-fd1f-e053-2a95a90ad34a.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74223-70074223-700-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
b0f15a0d-2782-492d-e053-2995a90ae4a0b11abfc2-ac84-fd1f-e053-2a95a90ad34a2020-10-05WarningsExact identifier
spl id: b0f15a0d-2782-492d-e053-2995a90ae4a0
spl set id: b11abfc2-ac84-fd1f-e053-2a95a90ad34a

Reported adverse events (FAERS/openFDA)#

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