FDA.reportPublic FDA data

Isopropyl Rubbing Alcohol 70 Percent

Manufacturer
Humco Holding Group, Inc.
Effective date
2020-06-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:18:28

Label at a glance#

ProductIsopropyl Rubbing Alcohol 70 Percent
Active ingredientISOPROPYL ALCOHOL
Label structure15 sections

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% by volume

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in.

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only.

  • Flammable, keep way from spark, heat and flame.

Ask a doctor before use for

OTC - ASK DOCTOR SECTION

  • deep wounds
  • animal bites
  • 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 1 week

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 accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY INFORMATION

  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  • will produce serious gastric disturbances if taken internally.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

Good Neighbor Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel NDC 46122-330-43 ISOPROPYL RUBBING ALCOHOL 70% USP First Aid Antiseptic 16 fl oz (1 pt) 473 mLPrincipal Display Panel NDC 46122-330-43 ISOPROPYL RUBBING ALCOHOL 70% USP First Aid Antiseptic 16 fl oz (1 pt) 473 mL

Health Mart Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HM70.jpgHM70.jpgHMHM

Sunmark Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SM70.jpgSM70.jpgSMSM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN3
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD3
808520isopropyl alcohol 70 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0395-9120-162022-07-29C16284748780-1e4f33bdf-ae93-d8a0-e053-dadaa90a6e4ePrivate Label Isopropyl Rubbing Alcohol 70 Percent, USP
0395-9120-282022-07-29C16284748780-1e4f33bdf-ae93-d8a0-e053-dadaa90a6e4ePrivate Label Isopropyl Rubbing Alcohol 70 Percent, USP
0395-9120-322022-07-29C16284748780-1e4f33bdf-ae93-d8a0-e053-dadaa90a6e4ePrivate Label Isopropyl Rubbing Alcohol 70 Percent, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0395-9120-16Isopropyl Rubbing Alcohol 70 Percent473 mL in 1 BOTTLELIQUID4733
0395-9120-28Isopropyl Rubbing Alcohol 70 Percent3800 mL in 1 BOTTLELIQUID38003
0395-9120-32Isopropyl Rubbing Alcohol 70 Percent946 mL in 1 BOTTLELIQUID9463

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0395-9120ISOPROPYL RUBBING ALCOHOL 70 PERCENT (ISOPROPYL ALCOHOL) LIQUID [HUMCO HOLDING GROUP, INC.]3Legacy NDC, 3 package rows20200622_60640d1a-07e0-fb0b-e053-2a91aa0ad402.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
0395-91200395-9120-16, 0395-9120-32, 0395-9120-28

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
ISOPROPYL ALCOHOLND2M416302ACTIB

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
a8850611-71c8-5e5e-e053-2995a90a492260640d1a-07e0-fb0b-e053-2a91aa0ad4022020-06-20WarningsExact identifier
spl id: a8850611-71c8-5e5e-e053-2995a90a4922
spl set id: 60640d1a-07e0-fb0b-e053-2a91aa0ad402

Reported adverse events (FAERS/openFDA)#

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