Dosage and administration
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 10 years of age when using this product to avoid swallowing.
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 10 years of age when using this product to avoid swallowing.
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
This is a hand sanitizer manufactured according to the FDA OTC Hand Sanitizer Monograph. The hand sanitizer is manufactured using only the following ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) and Center for Disease Control (CDC) recommendations:
Alcohol 70% v/v. Purpose: Antiseptic
Antiseptic, Hand Sanitizer
Hand Sanitizer to help reduce bacteria on the skin.
For external use only. Flammable. Keep away from heat or flame. Allergy Alert: Contains Tea Tree Oil.
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. 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.
glycerin, hydrogen peroxide, water, activated charcoal, carbomer 940, denatonium benzoate, tea tree oil
Uses
Hand rub to help reduce bacteria on the skin.
Directions
- Place enough product on hands to cover all surfaces. Rub hands until dry.
- Supervise children under 10 years of age when using this product to avoid swallowing.
General Label:
60 mL OR 2 oz. NDC: 80052-001-01:
240 mL OR 8 oz. NDC: 80052-001-02
3785 mL OR 128 oz. NDC: 80052-001-03
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 80052-001-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-66dc-a426-e053-dadaa90af4c2 | abfc7e71-2c4c-b4ef-e053-2995a90acce3 |
| 80052-001-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-66dc-a426-e053-dadaa90af4c2 | abfc7e71-2c4c-b4ef-e053-2995a90acce3 |
| 80052-001-03 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-66dc-a426-e053-dadaa90af4c2 | abfc7e71-2c4c-b4ef-e053-2995a90acce3 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80052-001-01 | Chimborazo Hand Sanitizer | 60 mL in 1 BOTTLE, PLASTIC | GEL | 60 | 2 | |
| 80052-001-02 | Chimborazo Hand Sanitizer | 240 mL in 1 BOTTLE, PUMP | GEL | 240 | 2 | |
| 80052-001-03 | Chimborazo Hand Sanitizer | 3786 mL in 1 BOTTLE, PUMP | GEL | 3786 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 80052-001 | 80052-001-01, 80052-001-02, 80052-001-03 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DENATONIUM BENZOATE | 4YK5Z54AT2 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| LAVENDER OIL | ZBP1YXW0H8 | IACT |
| TEA TREE OIL | VIF565UC2G | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CARBOMER 940 | 4Q93RCW27E | IACT |
| TRIETHYLAMINE | VOU728O6AY | IACT |
| ACTIVATED CHARCOAL | 2P3VWU3H10 | 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 |
|---|---|---|---|---|---|---|
| b6985b0a-3faf-c37b-e053-2a95a90a30c9 | abfc7e71-2c4c-b4ef-e053-2995a90acce3 | 2020-12-16 | Warnings | b6985b0a-3faf-c37b-e053-2a95a90a30c9 abfc7e71-2c4c-b4ef-e053-2995a90acce3 |