ISOPROPYL RUBBING ALCOHOL 50%
- Manufacturer
- Singhfam Corporation | Anicare Pharmaceuticals Pvt. Ltd
- Effective date
- 2015-08-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:43:17
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 Ingredients
Water(Aqua), Methyl Salicylate, FD&C Blue #1, FD&C Yellow #5
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PRINCIPAL DISPLAY PANEL
ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0857099005719 | GTIN-13: 0857099005719 EAN-13: 0857099005719 GTIN-12: 857099005719 UPC-A: 857099005719 GTIN storage (14 digits): 00857099005719 | isopropyl-rubbing-alcohol-wintergreen.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52920-130-41 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-42 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-43 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-44 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-45 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-46 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
| 52920-130-47 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-4d1d-f424-e053-dadaa90a57ce | ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52920-130-41 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | 1 | |
| 52920-130-42 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 177 mL in 1 BOTTLE, PLASTIC | LIQUID | 177 | 1 | |
| 52920-130-43 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | 1 | |
| 52920-130-44 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 296 mL in 1 BOTTLE, PLASTIC | LIQUID | 296 | 1 | |
| 52920-130-45 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 354 mL in 1 BOTTLE, PLASTIC | LIQUID | 354 | 1 | |
| 52920-130-46 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 414 mL in 1 BOTTLE, PLASTIC | LIQUID | 414 | 1 | |
| 52920-130-47 | ISOPROPYL RUBBING ALCOHOL 50%WITH WINTERGREEN | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 1 |
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 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | 1 | |
| FD&C YELLOW NO. 5 | INACTIVE INGREDIENT | I753WB2F1M | 1 | |
| METHYL SALICYLATE | INACTIVE INGREDIENT | LAV5U5022Y | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- ISOPROPYL RUBBING ALCOHOL 50% WITH WINTERGREEN
- Isopropyl Alcohol
- WATER
- METHYL SALICYLATE
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 5
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52920-130 | 52920-130-41, 52920-130-42, 52920-130-43, 52920-130-44, 52920-130-45, 52920-130-46, 52920-130-47 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| METHYL SALICYLATE | LAV5U5022Y | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | ACTIB |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CAPSULE, LIQUID FILLED / ORAL | 0.08 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | POWDER / TOPICAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SOLUTION / TOPICAL | 0.01 %w/w | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | LOZENGE / BUCCAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | PASTE, DENTIFRICE / DENTAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | SUPPOSITORY / VAGINAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SYRUP / ORAL | 0.05 mg/5ml | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, FILM COATED / ORAL | 1.68 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CAPSULE, COATED, EXTENDED RELEASE / ORAL | NA | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | GEL / TOPICAL | 0.05 %w/w | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | PASTE / DENTAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SOLUTION / DENTAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, SUGAR COATED / ORAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CONCENTRATE / ORAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | LIQUID / TOPICAL | NA | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | DOUCHE / VAGINAL | 0.05 %w/w | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CAPSULE, COATED PELLETS / ORAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, CHEWABLE / ORAL | 4.5 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CAPSULE, DELAYED RELEASE / ORAL | 2 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | FILM, SOLUBLE / ORAL | 0.04 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | FILM / SUBLINGUAL | 0.07 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET, EXTENDED RELEASE / ORAL | 4 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CONCENTRATE / BUCCAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, EXTENDED RELEASE / ORAL | 2.03 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | LOTION / TOPICAL | NA | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | CAPSULE / ORAL | 16 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | LIQUID / ORAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | POWDER, FOR SOLUTION / ORAL | 0.04 mg/5ml | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET / SUBLINGUAL | 0.11 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SHAMPOO / TOPICAL | 0.75 %w/w | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | CREAM / TOPICAL | 0.01 %w/w | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET / BUCCAL | 0.11 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, DELAYED RELEASE / ORAL | 3 mg | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | PASTE, DENTIFRICE / DENTAL | 1.1 %w/w | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | SYRUP / ORAL | 0.1 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | CAPSULE, EXTENDED RELEASE / ORAL | 0.26 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SOLUTION / RECTAL | 0.01 %w/v | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | LOZENGE / ORAL | 53 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET, SUGAR COATED / ORAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | ELIXIR / ORAL | 0.15 mg | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | TABLET / ORAL | 10 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET, FILM COATED / ORAL | 0.16 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | MOUTHWASH / BUCCAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SOAP / TOPICAL | 0.01 %w/w | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET / SUBLINGUAL | 0.03 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | CAPSULE / ORAL | 652 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SOLUTION / ORAL | 1.13 mg/15ml | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET / ORAL | 27.53 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET, DELAYED RELEASE / ORAL | 0.01 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | ELIXIR / ORAL | NA | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | POWDER / TOPICAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | TABLET, COATED / ORAL | 0.52 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | SUSPENSION / ORAL | NA | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | POWDER, FOR SUSPENSION / ORAL | 1 mg/5ml | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | DOUCHE / VAGINAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET / ORAL | 180 mg | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | OINTMENT / TOPICAL | 0.01 %w/w | ||
| METHYL SALICYLATE | METHYL SALICYLATE | LAV5U5022Y | POWDER, DENTIFRICE / DENTAL | NA | ||
| FD&C YELLOW NO. 5 | FD&C YELLOW NO. 5 | I753WB2F1M | TABLET, COATED / ORAL | 7.93 mg | ||
| FD&C BLUE NO. 1 | FD&C BLUE NO. 1 | H3R47K3TBD | SUSPENSION / ORAL | 1 mg |
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 |
|---|---|---|---|---|---|---|
| 1d0b5bfe-3dd0-43be-e054-00144ff8d46c | c6d5896a-56b1-41f2-9c06-e8ffcfdf7e50 | 2015-08-11 | Warnings | 1d0b5bfe-3dd0-43be-e054-00144ff8d46c c6d5896a-56b1-41f2-9c06-e8ffcfdf7e50 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
