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| Product NDC Code | 73950-004 | ||||
|---|---|---|---|---|---|
| Drug Name | Hand sanitizer |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | GEL | ||||
| RxCUI drug identifier | 581660 | ||||
| Application Number | part333E | ||||
| Labeler Name | MINISO DEPOT CA, INC. | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Ethyl Alcohol 62%
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions: Wet hands thoroughly with product and allow to dry without wiping.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients: Water, Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Tocopheryl Acetate, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Maltodextrin, Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays(Corn)Starch, Hydroxypropyl MethylCellulose, Ultramarines(CI 77007), FD&C Yellow No.5(Cl 19140), FD&C Blue No.1(Cl 42090).
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses Decrease bacteria on hands
Purpose
Information about the drug product’s indications for use.Purpose Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.Hand Sanitizer ETHYL ALCOHOL FD&C YELLOW NO. 5 ULTRAMARINE BLUE AMINOMETHYLPROPANOL FD&C BLUE NO. 1 HYPROMELLOSE, UNSPECIFIED .ALPHA.-LACTOSE SUCROSE MALTODEXTRIN ALOE VERA LEAF PROPYLENE GLYCOL ALCOHOL ALCOHOL WATER GLYCERIN CARBOMER INTERPOLYMER TYPE A (55000 CPS) .ALPHA.-TOCOPHEROL ACETATE STARCH, CORN MICROCRYSTALLINE CELLULOSE
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.image of bottle label
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep it out of reach of children.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if irritation or redness develop.If swallowed,get medical help or contact a doctor right away.
Storage and handling
Information about safe storage and handling of the drug product.Storage: Flammable,Avoid direct sunlight and keep away from fire.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings For external use only. Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API