Storage and handling
Other information store at a temperature below 110 F(43 C)
Hand Sanitizer - Merci Handy Corporation
- Manufacturer
- Merci Handy Corporation
- Effective date
- 2019-02-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:02:07
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Alcohol 67%
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
for handwashing to decrease bacteria on the skin.
WARNINGS SECTION
Warnings
For external use only. Flammable, keep away from fire or flame.
Do not use in the eyes.In case of contact, flush eyes with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if
- irritation and redness develop.
- condition persists for more than 72 hours
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
wet hand thoroughly with product and allow to dry without wiping
STORAGE AND HANDLING SECTION
Other information
store at a temperature below 110 F(43 C)
INACTIVE INGREDIENT SECTION
Inactive ingredients
water(aqua), aloe vera leaf juice, glycerin, propylene glycol, fragrance(parfum), acrylates/C30-10 alkyl acrylate crosspolymer, aminomethyl propanol, mannitol, microcrystalline cellulose, sucrose, corn(zea mays) starch, hydroxpropyl methyl cellulose, tocopheryl acetate, denatonium benzonate, maltodextrin, benzyl benzoate, hexyl cinnamal, limonene, linalool, Ferric Ferrocyanide, D&C Red No.30, D&C Red No.33, FD&C Blue No.1.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72866-105-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-b060-d83d-e063-dadaa90ab31f | 828a836d-dace-e387-e053-2991aa0a7261 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72866-105-01 | Hand Sanitizer | 30 mL in 1 BOTTLE | GEL | 30 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ETHYL ALCOHOL
- D&C RED NO. 30
- LIMONENE, (+)-
- BENZYL BENZOATE
- FERRIC FERROCYANIDE
- DENATONIUM BENZOATE
- MALTODEXTRIN
- .ALPHA.-HEXYLCINNAMALDEHYDE
- PROPYLENE GLYCOL
- MANNITOL
- ALCOHOL
- WATER
- ALOE VERA LEAF
- GLYCERIN
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- AMINOMETHYLPROPANOL
- CELLULOSE, MICROCRYSTALLINE
- SUCROSE
- STARCH, CORN
- .ALPHA.-TOCOPHEROL ACETATE
- HYPROMELLOSES
- D&C RED NO. 33
- FD&C BLUE NO. 1
- LINALOOL, (+)-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72866-105 | 72866-105-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 828a836d-dacf-e387-e053-2991aa0a7261 | 828a836d-dace-e387-e053-2991aa0a7261 | 2019-02-23 | Warnings | 828a836d-dacf-e387-e053-2991aa0a7261 828a836d-dace-e387-e053-2991aa0a7261 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.