OTC Medication Information: Hand Sanitizer, Glitter Fever

HAND SANITIZER, GLITTER FEVER- alcohol gel
Merci Handy Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

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:

Label4
(click image for full-size original)

HAND SANITIZER, GLITTER FEVER
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:72866-009
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 670 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
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
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72866-009-30 30 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/01/2020 06/30/2025
Labeler — Merci Handy Corporation (118006306)

Revised: 11/2022 Merci Handy Corporation

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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