Soho Fresh Rubbing Alcohol

Manufacturer: ESSAAR INC.
Effective date: 2020-06-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:19

Label at a glance#

ProductSoho Fresh Rubbing Alcohol

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

to decrease germs in minor cuts and scrapes

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% by volume

Purpose

OTC - PURPOSE SECTION

Uses

INDICATIONS & USAGE SECTION

to decrease germs in minor cuts and scrapes

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable, Keep away from fire of flame.

produce serious gastric disturbances if taken internally

Do not use

OTC - DO NOT USE SECTION

as a substitute for grain or ethyl alcohol-on irritated skin

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep only or puncture wounds, serious burns

When using this product

OTC - WHEN USING SECTION

avoid getting into eyes or on
mucous membranes
use only in a well ventilated area

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or swelling develops on the skin
pain persists or increase or if infection occurs

If pregnant or breast feeding,

PREGNANCY SECTION

ask a health professional before use

Keep out of reach of children,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

in case of an accidental ingestion seek professional assistance, or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to skin directly or with clean gauze, cotton or swab

For rubbing apply liberally and rub with hands

Other information

SPL UNCLASSIFIED SECTION

Keep bottle tightly closed

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	1
582753	ethanol 0.7 ML/ML Topical Solution	SCD	1
582753	ethanol 70 % Topical Solution	SY	1
582753	ethyl alcohol 70 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78533-001-33	2022-01-28	C162847	48780-1	d6a99b39-a905-a426-e053-dadaa90af4c2	Soho Fresh Rubbing Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78533-001-33	Soho Fresh Rubbing Alcohol	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
78533-001	SOHO FRESH RUBBING ALCOHOL (ALCOHOL) LIQUID [ESSAAR INC.]	1	Legacy NDC, 1 package rows	20200619_a85db976-df62-b5d4-e053-2995a90ae427.zip

Products#

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

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

Soho Fresh Rubbing Alcohol
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78533-001	78533-001-33

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
ALCOHOL	3K9958V90M	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
a85db494-349f-5e86-e053-2a95a90a7967			a85db976-df62-b5d4-e053-2995a90ae427	2020-06-18	Warnings	Exact identifier spl id: a85db494-349f-5e86-e053-2a95a90a7967 spl set id: a85db976-df62-b5d4-e053-2995a90ae427

Reported adverse events (FAERS/openFDA)#

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