Dosage and administration
wet hands thoroughly with product brisky rub hands together until dry Supervise children under 6 years in the use of this product.
wet hands thoroughly with product brisky rub hands together until dry Supervise children under 6 years in the use of this product.
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
This is a hand sanitizer manufactured according to the
Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
Alcohol 70% v/v. Purpose: Antiseptic
Antiseptic, Hand Sanitizer
for hand washing to decrease bacteria on the skin.
recommended for repeated use.
For external use only. Flammable. Keep away from heat or flame
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
auqa, propylene glycol, fragrance green tea, carbomer, triethanolamine, glycerin
Use: Rewording
Directions: rewording
70 mL NDC: 78819-101-01
100 mL NDC: 78819-101-02
250 mL NDC: 78819-101-03
500 mL NDC: 78819-101-04
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78819-101-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-48de-a426-e053-dadaa90af4c2 | a7a6d24e-359a-d2a0-e053-2a95a90a5475 |
| 78819-101-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-48de-a426-e053-dadaa90af4c2 | a7a6d24e-359a-d2a0-e053-2a95a90a5475 |
| 78819-101-03 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-48de-a426-e053-dadaa90af4c2 | a7a6d24e-359a-d2a0-e053-2a95a90a5475 |
| 78819-101-04 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-48de-a426-e053-dadaa90af4c2 | a7a6d24e-359a-d2a0-e053-2a95a90a5475 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78819-101-01 | Hand Sanitizer | 70 mL in 1 BOTTLE | GEL | 70 | 3 | |
| 78819-101-02 | Hand Sanitizer | 100 mL in 1 BOTTLE | GEL | 100 | 3 | |
| 78819-101-03 | Hand Sanitizer | 250 mL in 1 BOTTLE | GEL | 250 | 3 | |
| 78819-101-04 | Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 78819-101 | 78819-101-01, 78819-101-02, 78819-101-03, 78819-101-04 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER 940 | 4Q93RCW27E | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| GREEN TEA LEAF | W2ZU1RY8B0 | 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 |
|---|---|---|---|---|---|---|
| b1b26da3-bed8-2b9a-e053-2a95a90afa63 | a7a6d24e-359a-d2a0-e053-2a95a90a5475 | 2020-10-15 | Warnings | b1b26da3-bed8-2b9a-e053-2a95a90afa63 a7a6d24e-359a-d2a0-e053-2a95a90a5475 |
Adverse event summaries are temporarily unavailable. Other product information remains available.