Dosage and administration
• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.
MEDICAP HAND SANITIZER
- Manufacturer
- Zurich Pharma Inc
- Effective date
- 2020-04-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:34:35
Label at a glance#
ProductMEDICAP HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections
Storage and handling
• Store between 15-30C (59-86F) • Avoid freezing and excessive heat above 40C (104F)
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient[s]
Alcohol 80% v/v
Purpose
Antiseptic
Use[s]
• Hand sanitizer to help reduce bacteria that potentially can cause disease.
• For use when soap and water are not available.
Warnings
For external use only. 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, 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.
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
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.
Other information
• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)
INACTIVE INGREDIENT SECTION
Inactive ingredients: glycerin, hydrogen peroxide, distilled water
SPL UNCLASSIFIED SECTION
Topical Solution
Non-sterile Solution
Product of Canada
Distributed by:
Medicap Laboratories,
Tampa, FL 33610. +1-844-972-0220
Packaging
Products#
Every source-derived product name is available through these pages.
- MEDICAP HAND SANITIZER
- Alcohol
- GLYCERIN
- HYDROGEN PEROXIDE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74126-080 | 74126-080-59 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 9e0bd349-69a5-4235-af5a-bde3dc84d938 | 1b9cd586-dd76-470e-afb8-40a797bec6a8 | 2021-07-20 | Warnings | 1b9cd586-dd76-470e-afb8-40a797bec6a8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.