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Nuvalu instant hand sanitizer original 8oz - Medication Information

Product NDC Code 76176-214
Drug Name

Nuvalu instant hand sanitizer original 8oz

Type Brand
Active Ingredients
Alcohol 70 ml/100ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581662
Application Number part333A
Labeler Name Ningbo Liyuan Daily Chemical Products Co., Ltd.
Packages
Package NDC Code Description
76176-214-12 236 ml in 1 bottle, plastic (76176-214-12)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active Ingredient Ethyl Alcohol 70 percent

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 Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: water (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocophereyl acetate (vitamin E), aloe barbadensis leaf juice

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 Helps reduce bacteria on the 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.
NUVALU INSTANT HAND SANITIZER ORIGINAL 8OZ ETHYL ALCOHOL ALCOHOL ALCOHOL ALOE VERA LEAF PROPYLENE GLYCOL WATER CARBOMER 934 GLYCERIN CUPRIC BIS(TRIETHANOLAMINE) .ALPHA.-TOCOPHEROL ACETATE

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.
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 out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Store below 106 Fahrenheit (41 Degree Celsius) May discolor certain fabrics or surfaces.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.

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 Flammable. Keep away from fire or flame. For external use only.

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