Dosage and administration
wet hands thoroughly with product and allow to dry without wiping
Hand Sanitizer, Glitter Fever
- Manufacturer
- Merci Handy Corporation
- Effective date
- 2022-11-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:46:07
Label at a glance#
ProductHand Sanitizer, Glitter Fever
Active ingredientALCOHOL
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Alcohol 67%
Purpose
Antiseptic
Use
- for handwashing to decrease bacteria on the skin
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.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping
Other information
store at a temperature below 110° F (43° C)
Inactive ingredients
Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Denatonium Benzoate, Tocopheryl Acetate,
Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Fluorphlogopite, Coumarin, Limonene, Alpha-Isomethyl Ionone, Cinnamyl Alcohol, Isoeugenol, Titanium Dioxide, FD&C Yellow No. 5, Iron Oxides FD&C Red No. 4.
QUESTIONS OR COMMENTS?
(646)-358-3432
Package Labeling:
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer, Glitter Fever
- ALCOHOL
- WATER
- ALOE VERA LEAF
- GLYCERIN
- PROPYLENE GLYCOL
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- AMINOMETHYLPROPANOL
- MANNITOL
- MICROCRYSTALLINE CELLULOSE
- SUCROSE
- CORN
- DENATONIUM BENZOATE
- .ALPHA.-TOCOPHEROL ACETATE
- MALTODEXTRIN
- HYPROMELLOSE, UNSPECIFIED
- POTASSIUM SORBATE
- SODIUM BENZOATE
- COUMARIN
- LIMONENE, (+)-
- ISOMETHYL-.ALPHA.-IONONE
- CINNAMYL ALCOHOL
- ISOEUGENOL
- TITANIUM DIOXIDE
- FD&C YELLOW NO. 5
- FERRIC OXIDE RED
- FD&C RED NO. 4
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72866-009 | 72866-009-30 |
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 |
|---|---|---|---|---|---|---|
| eea07c75-2fed-2cae-e053-2a95a90a08b0 | 957c51c2-ab0b-4785-bba7-6f4f83e38dae | 2022-11-29 | Warnings | eea07c75-2fed-2cae-e053-2a95a90a08b0 957c51c2-ab0b-4785-bba7-6f4f83e38dae |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.