Storage and handling
Other Information For your protection, this bottle has an imprinted seal around the cap. Do not use if tamper evident seal is missing, tampered, broken, or destroyed.
Bortons Ethyl Rubbing Alcohol
- Manufacturer
- J-Mark International Inc.
- Effective date
- 2010-05-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 22:24:31
Label at a glance#
ProductBortons Ethyl Rubbing Alcohol
Active ingredientALCOHOL
Label structure11 sections
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients Purpose
Ethyl Alcohol 82 percent Antiseptic
OTC - PURPOSE SECTION
Uses
First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.
WARNINGS SECTION
Warnings
Flammable. Keep away from fire or flame. For external use only. Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
Clean the affected area. Apply a small amount of this product on the area 1 ti 3 times daily. May be covered with a sterile bandage.
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Camphor, Water
STORAGE AND HANDLING SECTION
Other Information
For your protection, this bottle has an imprinted seal around the cap. Do not use if tamper evident seal is missing, tampered, broken, or destroyed.
DESCRIPTION SECTION
Distributed by/Distribuido por
J-MARK International Inc.
0819-03925
Panama
Made In/Hecho en Panama
Expiration Date/Fecha de Expiracion 12/20/15
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Borton's ETHYL RUBBING ALCOHOL 82 percent By Volume FIRST AID ANTISEPTIC Net Contents 16 fl oz (473 ml)
CONTROLLED SUBSTANCE SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50790-100-16 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cda7-621f-e053-dbdaa90a74ad | Borton's Ethyl Rubbing Alcohol |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50790-100-16 | Bortons Ethyl Rubbing Alcohol | 473 mL in 1 BOTTLE | LIQUID | 473 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ALCOHOL | ACTIVE INGREDIENT | 3K9958V90M | 4 | |
| ALCOHOL | ACTIVE MOIETY | 3K9958V90M | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 4 |
Products#
Every source-derived product name is available through these pages.
- Bortons Ethyl Rubbing Alcohol
- ALCOHOL
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50790-100 | 50790-100-16 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| a43d8b25-96ec-4daf-8ab8-3958b6765e05 | 87b6d362-ce77-446b-a132-964da574b40a | 2010-05-14 | Warnings | a43d8b25-96ec-4daf-8ab8-3958b6765e05 87b6d362-ce77-446b-a132-964da574b40a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.