Indications and uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Sani Stix
- Manufacturer
- X Auto Inc. | Doehler USA Inc.
- Effective date
- 2021-12-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:45:52
Label at a glance#
ProductSani Stix
Active ingredientALCOHOL
Label structure7 sections
Dosage and administration
• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age whenusing this product to avoid swallowing.
Label contents#
Full prescribing information#
Active ingredients
Ethanol alcohol 71.5%
Purpose
Antiseptic
Uses:
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
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 whenusing this product to avoid swallowing.
Other information:
• Store between 15-30C (59-86F) • Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients:
glycerin, hydrogen peroxide, purified water USP
Package Labeling:
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5eb9f24b-9328-475e-af0a-18021935eb6a | Product name | 1 | 20180220 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79245-000-00 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-9e18-d8a0-e053-dadaa90a6e4e | Sani Stix |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79245-000-00 | Sani Stix | 36 in 1 PACKAGE | GEL | 36 | 3 | |
| 79245-000-00 | Sani Stix | 3.5 mL in 1 POUCH | GEL | 3.5 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Sani Stix
- ALCOHOL
- GLYCERIN
- HYDROGEN PEROXIDE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79245-000 | 79245-000-00 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
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 |
|---|---|---|---|---|---|---|
| afd6af4b-f965-3898-e053-2995a90a8aae | 4ca02372-1a8a-46ff-a0f6-58dd33d7c499 | 2021-12-22 | Warnings | afd6af4b-f965-3898-e053-2995a90a8aae 4ca02372-1a8a-46ff-a0f6-58dd33d7c499 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.