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| Product NDC Code | 41366-050 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Hand sanitizer |
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| Type | Generic | ||||||
| Active Ingredients |
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| Route | EXTRACORPOREAL | ||||||
| Dosage Form | GEL | ||||||
| RxCUI drug identifier | 581662 | ||||||
| Application Number | M003 | ||||||
| Labeler Name | Zhejiang Meimi Technology Co., Ltd. | ||||||
| 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(s) Ethyl Alcohol 70% v/v
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 Put a dime sized drop onto hands and rub together briskly until dry.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, yellow 6, red 4.
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.Use Uses hand sanitizer to help reduce bacteria on skin.
Purpose
Information about the drug product’s indications for use.Purpose Antimicrobial
Spl product data elements
Usually a list of ingredients in a drug product.Hand Sanitizer Hand Sanitizer FD&C YELLOW NO. 6 FD&C RED NO. 4 PROPYLENE GLYCOL TROLAMINE WATER ALCOHOL ALCOHOL GLYCERIN CARBOMER 940 PUMPKIN
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.Package Label - Principal Display Panel 59 mL in 1 BOTTLE NDC: 41366-050-01 59 mL in 1 BOTTLE NDC: 41366-050-02 59ml label 59ml label
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.Do not use Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
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 out of reach of children. Supervise children under 6 years of age when using this product to avoid swallowing. If swallowed, get medical help or contact a Poison Control Center right away.
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, excessive redness or rash develops.
Storage and handling
Information about safe storage and handling of the drug product.Other information Store below 110℉(43℃).
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. Flammable. Keep away from heat or flame.
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