Isopropyl Rubbing Alcohol 70%
- Manufacturer
- Universal Distribution Center LLC | Jell Pharmaceuticals Pvt. Ltd. | Jell Pharmaceuticals Pvt Ltd.
- Effective date
- 2025-03-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:56:43
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients (by volume)
Isopropyl alcohol (70% conc.)
OTC - PURPOSE SECTION
Purpose
First aid antiseptic
INDICATIONS & USAGE SECTION
Uses
- first aid to help prevent the risk of infection in minor cuts, scrapes and burns
WARNINGS SECTION
Warnings
For external use only; flammable, keep away from fire or flame, heat, spark, electrical
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- deep punctured wounds, animal bites or serious burns
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
OTC - STOP USE SECTION
Stop using this product if
- condition persists or gets worse
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all drugs out of the reach of children
In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately
DOSAGE & ADMINISTRATION SECTION
Directions
- clean effected area
- apply small amount of this product on the area 1-3 times daily
- may be covered with a sterile bandage
- if bandaged, let dry first
SPL UNCLASSIFIED SECTION
Other information
- store at room temperature
- does not contain, nor is intended as a substitute for grain or ethyl alcohol
- will produce serious gastric disturbance if taken internally
INACTIVE INGREDIENT SECTION
Inactive ingredient
Water(Aqua)
SPL UNCLASSIFIED SECTION
PRINCIPAL DISPLAY PANEL
ISOPROPYL RUBBING ALCOHOL 70%
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52000-803-01 | Isopropyl Rubbing Alcohol 70% | 177 mL in 1 BOTTLE, PLASTIC | LIQUID | 177 | 1 | |
| 52000-803-02 | Isopropyl Rubbing Alcohol 70% | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | 1 | |
| 52000-803-03 | Isopropyl Rubbing Alcohol 70% | 296 mL in 1 BOTTLE, PLASTIC | LIQUID | 296 | 1 | |
| 52000-803-04 | Isopropyl Rubbing Alcohol 70% | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | 1 | |
| 52000-803-05 | Isopropyl Rubbing Alcohol 70% | 355 mL in 1 BOTTLE, PLASTIC | LIQUID | 355 | 1 | |
| 52000-803-06 | Isopropyl Rubbing Alcohol 70% | 414 mL in 1 BOTTLE, PLASTIC | LIQUID | 414 | 1 | |
| 52000-803-08 | Isopropyl Rubbing Alcohol 70% | 946 mL in 1 BOTTLE, PLASTIC | LIQUID | 946 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Isopropyl Rubbing Alcohol 70%
- Isopropyl Alcohol
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52000-803 | 52000-803-04, 52000-803-01, 52000-803-02, 52000-803-03, 52000-803-05, 52000-803-06, 52000-803-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Isopropyl Rubbing Alcohol 70% | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 2f988951-39e7-ec02-e063-6294a90aaad7 | 2025-03-05 | Warnings | 52000-803-01 52000-803-03 52000-803-05 52000-803-04 52000-803-06 52000-803-02 52000-803-08 52000-803 52000080305 52000080302 52000080301 52000080304 52000080306 52000080303 52000080308 2f98851f-6667-ec36-e063-6294a90af00c 2f988951-39e7-ec02-e063-6294a90aaad7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
