Dosage and administration
Wet hand thoroughly and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.
Daisy DND
- Manufacturer
- Daisy Nail Product Inc.
- Effective date
- 2020-06-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:17:35
Label at a glance#
ProductDaisy DND
Active ingredientALCOHOL
Label structure9 sections
Storage and handling
Store between 20°C-25°C (68-77°F). May discolor certain fabrics and surfaces.
Label contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 75% v/v.
Purpose
Antiseptic
Use[s]
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only- hands.
Flammable, keep away from heat or flame.
Do not use
- in children less than 2 months of age
- on open skin wounds
When using this product
- keep out of eyes, in case of contact with eyes, rinse eyes thoroughly with water.
- avoid contact with broken skin.
- do not inhale or ingest.
Stop use and ask a doctor if skin irritation develops.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Wet hand thoroughly and allow to dry without wiping.
- For children under 6, use only under adult supervision.
- Not recommended for infants.
Other information
- Store between 20°C-25°C (68-77°F).
- May discolor certain fabrics and surfaces.
Inactive ingredients
Glycerin, Bitandiol, Carboxypolymethylene, Vitamin E.
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78951-002-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-8ee1-a426-e053-dadaa90af4c2 | 423c20db-abb9-4a21-b3c0-ee3d82706e5f |
| 78951-002-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-8ee1-a426-e053-dadaa90af4c2 | 423c20db-abb9-4a21-b3c0-ee3d82706e5f |
| 78951-002-03 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-8ee1-a426-e053-dadaa90af4c2 | 423c20db-abb9-4a21-b3c0-ee3d82706e5f |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78951-002-01 | Daisy DND | 50 mL in 1 BOTTLE, PLASTIC | GEL | 50 | 1 | |
| 78951-002-02 | Daisy DND | 480 mL in 1 BOTTLE, PLASTIC | GEL | 480 | 1 | |
| 78951-002-03 | Daisy DND | 3785 mL in 1 BOTTLE, PLASTIC | GEL | 3785 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Daisy DND
- Alcohol
- GLYCERIN
- BUTANEDIOL (MIXED ISOMERS)
- CARBOXYPOLYMETHYLENE
- .ALPHA.-TOCOPHEROL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78951-002 | 78951-002-01, 78951-002-02, 78951-002-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| BUTANEDIOL (MIXED ISOMERS) | TMS4MGA0H4 | IACT |
| CARBOXYPOLYMETHYLENE | 0A5MM307FC | IACT |
| .ALPHA.-TOCOPHEROL | H4N855PNZ1 | 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 |
|---|---|---|---|---|---|---|
| d104a6dc-d228-4ddb-b798-78ebfb5ecb7d | 423c20db-abb9-4a21-b3c0-ee3d82706e5f | 2020-06-10 | Warnings | d104a6dc-d228-4ddb-b798-78ebfb5ecb7d 423c20db-abb9-4a21-b3c0-ee3d82706e5f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.