FDA.reportPublic FDA data

Natural Care Isopropyl Alcohol

Manufacturer
Dr. Natural LLC
Effective date
2020-09-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:45

Label at a glance#

ProductNatural Care Isopropyl Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Indications and uses

helps prevent the risk of infection in: minor cuts  scrapes burns

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% (v/v)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

helps prevent the risk of infection in:

  • minor cuts 
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only 

Flammable

  • keep away from fire or flame, heat, spark, electrical

Ask a doctor before use 

OTC - ASK DOCTOR SECTION

for deep or puncture wounds, animals bites or serious burns

When using this product 

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not inhale 
  • do not apply over large areas of the body
  • do not use longer then 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

If swallowed get medical help or contact a Poison Control Center right away.

Caution - Fumes can be acutely irritation to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

  • 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

water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Updated LabelUpdated Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN1
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD1
808520isopropyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78261-000-162022-01-28C16284748780-1d6a99b39-af72-a426-e053-dadaa90af4c2Natural Care Isopropyl Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78261-000-16Natural Care Isopropyl Alcohol473 mL in 1 BOTTLELIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78261-000NATURAL CARE ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [DR. NATURAL LLC]1Legacy NDC, 1 package rows20200919_af993a49-a981-193b-e053-2995a90a40ef.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
78261-00078261-000-16

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
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
af992e1b-e5b6-a8f1-e053-2995a90af96baf993a49-a981-193b-e053-2995a90a40ef2020-09-18WarningsExact identifier
spl id: af992e1b-e5b6-a8f1-e053-2995a90af96b
spl set id: af993a49-a981-193b-e053-2995a90a40ef

Reported adverse events (FAERS/openFDA)#

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