Dosage and administration
• apply a small portion on your hands, rub well and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing • use only as directed
• apply a small portion on your hands, rub well and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing • use only as directed
• Store in a dry place, well-vented and out of direct light • Store between 59-86°F (15- 30°C) • Avoid freezing and excessive heat above 104°F (40°C) • May discolor certain fabrics or surfaces
This is a hand sanitizer manufactured under OTC Monograph not final using only the following ingredients:
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
Alcohol 80% v/v. Purpose: Antiseptic
Antiseptic, Hand Sanitizer
• to decrease bacteria on the skin that could cause disease
• recommended for repeated use.
For external use only. Flammable. Keep away from heat or flame
• in children less than 2 months of age
• on Open Skin Wounds
When using this product:
• avoid contact with eyes, ears, and mouth. If contact occurs, rinse thoroughly with water
• avoid contact with broken skin
• avoid inhalation
• if inhaled for prolonged period, seek immediate medical attention
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.
• Keep away from pets.
• apply a small portion on your hands, rub well and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing
• use only as directed
• Store in a dry place, well-vented and out of direct light
• Store between 59-86°F (15- 30°C)
• Avoid freezing and excessive heat above 104°F (40°C)
• May discolor certain fabrics or surfaces
Water (Aqua), Glycerin, Hypromellose
IQT Hand Sanitizer (gel) 264 gal (1,000,000 mL) NDC: 80189-101-01
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 80189-101 | 80189-101-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
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 |
|---|---|---|---|---|---|---|
| dd07102a-9829-c872-e053-2995a90a3883 | aee75d71-10a8-7c0b-e053-2995a90a1c7a | 2022-03-31 | Warnings | aee75d71-10a8-7c0b-e053-2995a90a1c7a |
Adverse event summaries are temporarily unavailable. Other product information remains available.