Isopropyl Rubbing Alcohol 50%
- Manufacturer
- Universal Distribution Center LLC
- Effective date
- 2024-10-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-06-01 00:41:46
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients (by volume)
Isopropyl alcohol (50% 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 50%
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 |
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52000-008-01 | Isopropyl Rubbing Alcohol 50% | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | 5 | |
| 52000-008-02 | Isopropyl Rubbing Alcohol 50% | 177 mL in 1 BOTTLE, PLASTIC | LIQUID | 177 | 5 | |
| 52000-008-03 | Isopropyl Rubbing Alcohol 50% | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | 5 | |
| 52000-008-04 | Isopropyl Rubbing Alcohol 50% | 296 mL in 1 BOTTLE, PLASTIC | LIQUID | 296 | 5 | |
| 52000-008-05 | Isopropyl Rubbing Alcohol 50% | 355 mL in 1 BOTTLE, PLASTIC | LIQUID | 355 | 5 | |
| 52000-008-06 | Isopropyl Rubbing Alcohol 50% | 414 mL in 1 BOTTLE, PLASTIC | LIQUID | 414 | 5 | |
| 52000-008-07 | Isopropyl Rubbing Alcohol 50% | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ISOPROPYL ALCOHOL | ACTIVE INGREDIENT | ND2M416302 | 1 | |
| ISOPROPYL ALCOHOL | ACTIVE MOIETY | ND2M416302 | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Isopropyl Rubbing Alcohol 50%
- Isopropyl Alcohol
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52000-008 | 52000-008-01, 52000-008-02, 52000-008-03, 52000-008-04, 52000-008-05, 52000-008-06, 52000-008-07 |
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 |
|---|---|---|---|---|---|---|
| a723b6de-4725-4f10-b4ab-3bbca4d65440 | 010a9d81-4039-441b-b478-41ccf527e4df | 2024-10-17 | Warnings | a723b6de-4725-4f10-b4ab-3bbca4d65440 010a9d81-4039-441b-b478-41ccf527e4df |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
