Indications and uses
• for preparation of the skin prior to injection • first aid to decrease germs in minor cuts, scrapes and burns
Up and Up alcohol
- Manufacturer
- Target Corporation
- Effective date
- 2013-12-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 22:37:54
Label at a glance#
ProductUp and Up alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections
Dosage and administration
Apply to skin as needed. Discard after single use.
Storage and handling
Protect from freezing and avoid excessive heat
Label contents#
Full prescribing information#
Active ingredient
Isopropyl alcohol, 70% v/v
Purpose
Antiseptic
Uses
- for preparation of the skin prior to injection
- first aid to decrease germs in minor cuts, scrapes and burns
Warnings
For external use only.
When using this product
- do not get into eyes
- do not 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 ask a doctor if
condition persists or gets worse or lasts for more than 72 hours. Do not use longer than 1 week unless directed by a doctor.
Flammable, keep away from fire or flame.
- Do not use with electrocautery procedures
- Use only in a well ventilated area; fumes may be toxic.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply to skin as needed. Discard after single use.
Other information
Protect from freezing and avoid excessive heat
Inactive ingredients
Water
Package/Label Principal Display Panel
Up&Up
alcohol swabs
70% isopropyl alcohol
sterile
antiseptic for preparation of skin prior to injection
2-ply swabs
individually wrapped
100 COUNT
100 PADS – 1 1/8 in x 2 3/8 in (2.8 cm x 6 cm)
Package/Label Back
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 11673-809-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-a2a0-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11673-809-09 | Up and Up alcohol | 5 mL in 1 APPLICATOR | SWAB | 5 | 3 | |
| 11673-809-09 | Up and Up alcohol | 1 in 1 PACKET | SWAB | 1 | 3 | |
| 11673-809-30 | Up and Up alcohol | 100 in 1 BOX | SWAB | 100 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ISOPROPYL ALCOHOL | ACTIVE INGREDIENT | ND2M416302 | 3 | |
| ISOPROPYL ALCOHOL | ACTIVE MOIETY | ND2M416302 | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 3 |
Products#
Every source-derived product name is available through these pages.
- Up and Up alcohol
- Isopropyl Alcohol
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11673-809 | 11673-809-09, 11673-809-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ISOPROPYL ALCOHOL | ND2M416302 | 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 |
|---|---|---|---|---|---|---|
| 6d8cc502-22ba-4520-8fcb-2ae21a77413a | 24e35c69-31eb-421e-8655-db4dbd4b0a9f | 2013-12-26 | Warnings | 6d8cc502-22ba-4520-8fcb-2ae21a77413a 24e35c69-31eb-421e-8655-db4dbd4b0a9f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.