Storage and handling
Other information • Store between 59-86F (15-30C) • Avoid freezing and excessive heat above 140F (40C)
Hand Sanitizer
- Manufacturer
- Maryland Correctional Enterprises
- Effective date
- 2020-04-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:33:27
Label at a glance#
ProductHand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure14 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:
Isopropyl Alcohol >/= 70.1%
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Water, Betaine Anhydrous, Anionic Water Soluble Polymer,
Amino Methyl Propanol, DL Alpha Tocopherol Acetate
WARNINGS SECTION
For external use only. Flammable. Keep away from heat or flame
OTC - PURPOSE SECTION
Use[s] • Hand sanitizer to help reduce bacteria that potentially
can cause disease.
OTC - DO NOT USE SECTION
Do not use
• in children less than 2 months of age
• on open skin wounds
INDICATIONS & USAGE SECTION
For use when soap and water are not
available.
OTC - WHEN USING SECTION
When using this product keep out of eyes, ears, and mouth. In
case of contact with eyes, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
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.
DOSAGE & ADMINISTRATION SECTION
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
STORAGE AND HANDLING SECTION
Other information
• Store between 59-86F (15-30C)
• Avoid freezing and excessive heat above 140F (40C)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74689-000-16 | 2026-01-07 | C162847 | 48780-1 | c7ccaba7-28ce-fd44-e053-dadaa90aa01b | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 |
| 74689-000-32 | 2026-01-07 | C162847 | 48780-1 | c7ccaba7-28ce-fd44-e053-dadaa90aa01b | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 |
| 74689-000-16 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-28ce-fd44-e053-dadaa90aa01b | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 |
| 74689-000-32 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-28ce-fd44-e053-dadaa90aa01b | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Isopropyl Alcohol
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- BETAINE
- AMINOMETHYLPROPANOL
- WATER
- .ALPHA.-TOCOPHEROL ACETATE, DL-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74689-000 | 74689-000-32, 74689-000-16 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | ACTIB |
| BETAINE | 3SCV180C9W | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| WATER | 059QF0KO0R | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, DL- | WR1WPI7EW8 | 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 |
|---|---|---|---|---|---|---|
| c741a648-4a40-ddad-e053-2995a90ab030 | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 | 2021-07-16 | Warnings | a26956c4-96fa-b8e9-e053-2a95a90a3cb8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.