Indications and uses
To decrease bacteria on the skin that could cause disease - Recommended for repeated use.
To decrease bacteria on the skin that could cause disease - Recommended for repeated use.
Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision ■ Not recommended for infants.
Do not store above 105°F ■ May discolor some fabrics Harmful to wood finishes and plastics.
Ethyl Alcohol 70%
Antiseptic
To decrease bacteria on the skin that could cause disease - Recommended for repeated use.
For external use only: Hands.
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water ■ Avoid contact with broken skin ■ Do not inhale or ingest ■ Stop use and ask a doctor if: irritation and redness develop or condition persists for more than 72 hours.
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Wet hands thoroughly with product and allow to dry without wiping
For children under 6, use only under adult supervision ■ Not recommended for infants.
Do not store above 105°F ■ May discolor some fabrics
Harmful to wood finishes and plastics.
Deionized Water, Aloe Vera Gel (Aloe Barbadensis Leaf Juice), Carbomer, Triethanolamine, Vitamin E (Tocopheryl Acetate).
Distributed by Imperial Dade
Manufactured for Imperial Dade
255 Route 1 & 9
Jersey City, NJ 07306.
MADE IN USA
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71907-200-22 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-5de2-a426-e053-dadaa90af4c2 | PREMIUM GEL ALCOHOL HAND SANITIZER |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71907-200-22 | Premium Gel Alcohol Hand Sanitizer | 3.78 L in 1 BOTTLE | GEL | 3.78 | 1 | |
| 71907-200-22 | Premium Gel Alcohol Hand Sanitizer | 2 in 1 CASE | GEL | 2 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71907-200 | 71907-200-22 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| .ALPHA.-TOCOPHEROL | H4N855PNZ1 | IACT |
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 |
|---|---|---|---|---|---|---|
| d10b7f90-b278-4ddf-81c4-4df4e4e85210 | 9d1b926e-ba75-4d28-838e-ec40b1fee2d5 | 2020-07-30 | Warnings | d10b7f90-b278-4ddf-81c4-4df4e4e85210 9d1b926e-ba75-4d28-838e-ec40b1fee2d5 |
Adverse event summaries are temporarily unavailable. Other product information remains available.