TSC Rubbing Alcohol - 70% Isopropyl Alcohol

Manufacturer
TS Cosmetic Labs, Inc.
Effective date
2020-08-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:32

Label at a glance#

ProductTSC Rubbing Alcohol - 70% Isopropyl Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Dosage and administration

Directions: Clean affected area. Apply small amount of this product on the area 1-3 times daily. If bandaged, let dry first. May be covered with a sterile bandage.

Storage and handling

Other Information Store at room temperature. Does not contain, nor is intended as a substitute for grain or ethyl alcohol. If taken internally, serious gastric disturbances will result.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a Rubbing Alcohol consisting of 70% Isopropyl Alcohol.

This Rubbing Alcohol is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation):

  1. Isopropyl Alcohol (USP or meeting Criteria of USP) (70%, volume/volume (v/v))
  2. Purified water (30% v/v)

This firm does not add other active or inactive ingredients than those stated above.

Active Ingredient (by volume)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in minor cuts, scrapes and burns.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • deep or puncture wounds, animal bites or serious burns.

When using this product

OTC - WHEN USING SECTION

When using this product

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor

  • condition persists or gets worse.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If case of ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Clean affected area.
  • Apply small amount of this product on the area 1-3 times daily. If bandaged, let dry first. May be covered with a sterile bandage.

Other information

STORAGE AND HANDLING SECTION

Other Information

  • Store at room temperature.
  • Does not contain, nor is intended as a substitute for grain or ethyl alcohol.
  • If taken internally, serious gastric disturbances will result.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70% Isopropyl Rubbing Alcohol - 32 oz70% Isopropyl Rubbing Alcohol - 32 oz

NDC: 78056-770-32

32 oz | 946 mL

70% Isopropyl Rubbing Alcohol - 1 gal70% Isopropyl Rubbing Alcohol - 1 gal

NDC: 78056-770-01

1 Gal. | 3785 mL

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
78056-77078056-770-32, 78056-770-01

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
c7328ed3-a384-1cb5-e053-2a95a90a85a1ae4636e0-e10f-fe85-e053-2995a90a25702021-07-15WarningsExact identifier
spl set id: ae4636e0-e10f-fe85-e053-2995a90a2570

Reported adverse events (FAERS/openFDA)#

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