HANNA ISOPROPYL RUBBING ALCOHOL 70%

Manufacturer: Rainbow Co Ltd
Effective date: 2020-07-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:40

Label at a glance#

ProductHANNA ISOPROPYL RUBBING ALCOHOL 70%

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

isopropyl alcohol

INACTIVE INGREDIENT SECTION

WATER,

OTC - PURPOSE SECTION

Sterilization of hands and skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply an appropriate amount on your hands and rub well to dry.

WARNINGS SECTION

1. Do not use on the following body parts. A wide range of body parts and damaged skin around the eyes and ears, in the oral cavity (may have irritating effects)
2. If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.
1) Hypersensitivity symptoms such as rash, erythema, itching, and edema
2) Skin irritation symptoms

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	1
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	1
808520	isopropyl alcohol 70 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74247-0015-1	2021-07-23	C162847	48780-1	c7ccaba7-234f-fd44-e053-dadaa90aa01b	Drug Facts
74247-0015-2	2021-07-23	C162847	48780-1	c7ccaba7-234f-fd44-e053-dadaa90aa01b	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74247-0015-1	HANNA ISOPROPYL RUBBING ALCOHOL 70%	500 mL in 1 BOTTLE	LIQUID	500		1
74247-0015-2	HANNA ISOPROPYL RUBBING ALCOHOL 70%	1000 mL in 1 BOTTLE	LIQUID	1000		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74247-0015	HANNA ISOPROPYL RUBBING ALCOHOL 70% (ISOPROPYL RUBBING ALCOHOL) LIQUID [RAINBOW CO LTD]	1	Legacy NDC, 2 package rows	20200726_ab41ed73-c020-35c3-e053-2a95a90a0ec6.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

HANNA ISOPROPYL RUBBING ALCOHOL 70%
ISOPROPYL RUBBING ALCOHOL
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74247-0015	74247-0015-2, 74247-0015-1

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
ab41ed73-c01f-35c3-e053-2a95a90a0ec6			ab41ed73-c020-35c3-e053-2a95a90a0ec6	2020-07-25	Warnings	Exact identifier spl id: ab41ed73-c01f-35c3-e053-2a95a90a0ec6 spl set id: ab41ed73-c020-35c3-e053-2a95a90a0ec6

Reported adverse events (FAERS/openFDA)#

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