Isopropyl Rubbing Alcohol 50%

Manufacturer: MY IMPORTS LLC | Jell Pharmaceuticals Pvt. Ltd.
Effective date: 2024-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:45:01

Label at a glance#

ProductIsopropyl Rubbing Alcohol 50%

Active ingredientISOPROPYL ALCOHOL

Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (by volume)

Isopropyl alcohol (50% concentrate)

OTC - PURPOSE SECTION

Purpose

topical antimicrobial

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

Warnings

For external use only

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

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havedeep puncture wounds or serious burns

OTC - DO NOT USE SECTION

When using this product

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of an accidental ingestion, contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION

Directions

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

SPL UNCLASSIFIED SECTION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredient

Water

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL

ISOPROPYL RUBBING ALCOHOL 50%

TOPICAL ANTIMICROBIAL

12 FL.OZ (354 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616456	isopropyl alcohol 50 % Topical Solution	PSN	4
616456	isopropyl alcohol 0.5 ML/ML Topical Solution	SCD	4
616456	isopropyl alcohol 50 % Topical Solution	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51628-4232-1	Isopropyl Rubbing Alcohol 50%	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355	4
51628-4232-2	Isopropyl Rubbing Alcohol 50%	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	4
51628-4232-3	Isopropyl Rubbing Alcohol 50%	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51628-4232	ISOPROPYL RUBBING ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [MY IMPORTS LLC]	4	Current NDC, Legacy NDC, 3 package rows	20241220_d4d72406-067d-1f67-e053-2995a90a1a9f.zip

Products#

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

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

Isopropyl Rubbing Alcohol 50%
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51628-4232	51628-4232-1, 51628-4232-2, 51628-4232-3

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Isopropyl Rubbing Alcohol 50%	ISOPROPYL ALCOHOL	MY IMPORTS LLC	d4d72406-067d-1f67-e053-2995a90a1a9f	2024-12-18	Warnings	Exact identifier ndc (package): 51628-4232-3 ndc (package): 51628-4232-1 ndc (package): 51628-4232-2 ndc (product): 51628-4232 ndc11 (package): 51628423203 ndc11 (package): 51628423202 ndc11 (package): 51628423201 spl id: 29880318-13b3-2d0b-e063-6294a90a9263 spl set id: d4d72406-067d-1f67-e053-2995a90a1a9f

Reported adverse events (FAERS/openFDA)#

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