Dosage and administration
clean skin and apply a small amount of this product 1-3 daily on selected area as needed allow product to remain on skin surface until dry
Rubbing Alcohol
- Manufacturer
- Ningbo Pretty Tourism Manufacture Co., Ltd
- Effective date
- 2020-07-24
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:22:35
Label at a glance#
ProductRubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections
Storage and handling
Store at room temperature does not contain, nor is intended as a substitute for grain or ethyl alcohol keep bottle tightly closed
Label contents#
Full prescribing information#
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria and germs on skin. helps relieve minor muscular aches due to exertion
Warnings
For external use only. Flammable. Keep away from heat or flame. Not recommended for deep puncture wounds, animal bites or serious burns. If taken internally, serious gastric disturbances will result.
Do not use
- in children less than 2 months of age
- on open skin wounds
OTC - WHEN USING SECTION
- do not get into eyes
- do not apply over large areas of the body
- do not use longer than one week
OTC - STOP USE SECTION
Condition persists or gets worse
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- clean skin and apply a small amount of this product 1-3 daily on selected area as needed
- allow product to remain on skin surface until dry
Other information
- Store at room temperature
- does not contain, nor is intended as a substitute for grain or ethyl alcohol
- keep bottle tightly closed
Inactive ingredients
purified water (Aqua)
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75749-050-01 | 2023-01-30 | C162847 | 48780-1 | f386c64a-1e99-0266-e053-dadaa90a7c1a | ab323d6d-3c59-0d76-e053-2a95a90a63a2 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75749-050-01 | Rubbing Alcohol | 350 mL in 1 BOTTLE | LIQUID | 350 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Rubbing Alcohol
- Isopropyl Alcohol
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75749-050 | 75749-050-01 |
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 |
|---|---|---|---|---|---|---|
| ab323d32-7c34-0d6d-e053-2a95a90a6aef | ab323d6d-3c59-0d76-e053-2a95a90a63a2 | 2020-07-24 | Warnings | ab323d32-7c34-0d6d-e053-2a95a90a6aef ab323d6d-3c59-0d76-e053-2a95a90a63a2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.