Dosage and administration
wet hands thoroughly with product and allow to dry without wiping
Magic Pouch
- Manufacturer
- Merci Handy Corporation
- Effective date
- 2022-11-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:46:10
Label at a glance#
ProductMagic Pouch
Active ingredientALCOHOL
Label structure25 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, Hexyl Cinnamal, Benzyl Benzoate, Linalool, Limonene, Ferric Ferrocyanide, D&C Red No. 33, D&C Red No. 30, FD&C Blue No. 1.
QUESTIONS OR COMMENTS?
(646)-358-3432
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
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 Linalool, Limonene, Coumarin,
Hydroxycitronellal, Benzyl Benzoate, Titanium Dioxide, D&C Red No. 33, D&C Red No. 30.
QUESTIONS OR COMMENTS?
(646)-358-3432
Package Labeling:Kit
Package Labeling:NAMASTE
Package Labeling:GLITTER FEVER
Package Labeling:UNICORN EDITION
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72866-002 | MAGIC POUCH (ALCOHOL) KIT [MERCI HANDY CORPORATION] | 2 | Legacy NDC | 20221130_b232f228-3f85-a75a-e053-2a95a90a691b.zip |
| 72866-003 | MAGIC POUCH (ALCOHOL) KIT [MERCI HANDY CORPORATION] | 2 | Legacy NDC | 20221130_b232f228-3f85-a75a-e053-2a95a90a691b.zip |
| 72866-009 | MAGIC POUCH (ALCOHOL) KIT [MERCI HANDY CORPORATION] | 2 | Legacy NDC | 20221130_b232f228-3f85-a75a-e053-2a95a90a691b.zip |
| 72866-011 | MAGIC POUCH (ALCOHOL) KIT [MERCI HANDY CORPORATION] | 2 | Legacy NDC | 20221130_b232f228-3f85-a75a-e053-2a95a90a691b.zip |
Products#
Every source-derived product name is available through these pages.
- Magic Pouch
- ALCOHOL
- Hand Sanitizer, Namaste
- WATER
- ALOE VERA LEAF
- GLYCERIN
- PROPYLENE GLYCOL
- AMINOMETHYLPROPANOL
- MANNITOL
- MICROCRYSTALLINE CELLULOSE
- SUCROSE
- STARCH, CORN
- DENATONIUM BENZOATE
- .ALPHA.-TOCOPHEROL ACETATE
- MALTODEXTRIN
- HYPROMELLOSE, UNSPECIFIED
- POTASSIUM SORBATE
- SODIUM BENZOATE
- .ALPHA.-HEXYLCINNAMALDEHYDE
- BENZYL BENZOATE
- LINALOOL, (+/-)-
- LIMONENE, (+)-
- FERRIC FERROCYANIDE
- D&C RED NO. 33
- D&C RED NO. 30
- FD&C BLUE NO. 1
- Hand Sanitizer, Glitter Fever
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- CORN
- COUMARIN
- ISOMETHYL-.ALPHA.-IONONE
- CINNAMYL ALCOHOL
- ISOEUGENOL
- TITANIUM DIOXIDE
- FD&C YELLOW NO. 5
- FERRIC OXIDE RED
- FD&C RED NO. 4
- Hand Sanitizer, Unicorn Edition
- HYDROXYCITRONELLAL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72866-011 | 72866-011-01 |
| 72866-002 | 72866-002-30 |
| 72866-009 | 72866-009-30 |
| 72866-003 | 72866-003-30 |
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 |
|---|---|---|---|---|---|---|
| ee9fc539-255a-3a50-e053-2995a90a1a54 | b232f228-3f85-a75a-e053-2a95a90a691b | 2022-11-29 | Warnings | ee9fc539-255a-3a50-e053-2995a90a1a54 b232f228-3f85-a75a-e053-2a95a90a691b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.