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Traveltime instant hand sanitizer soothing aloe and vitamin e - Medication Information

Product NDC Code 74274-007
Drug Name

Traveltime instant hand sanitizer soothing aloe and vitamin e

Type Brand
Active Ingredients
Alcohol 65 ml/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 884783
Application Number part333E
Labeler Name Huizhou Bliss Commodity Co., Ltd
Packages
Package NDC Code Description
74274-007-01 59 ml in 1 bottle (74274-007-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Ethyl Alcohol 65%

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 enough product in palm to cover hands and rub hands together until dry. Children under 6 years of age should be supervised when applying product. Other information: Store below 110° (43℃) May discollor certain fabrics or surfaces.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, glycerin, propyene glycol, carbomer, sodium hydroxide, Aloe Barbadensis Leaf Juice, Fragrance

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 Hand sanitizer to help reduce bacteria on the skin.

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.
Traveltime Instant Hand Sanitizer Soothing Aloe and Vitamin E Alcohol ALCOHOL ALCOHOL WATER CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) GLYCERIN PROPYLENE GLYCOL SODIUM HYDROXIDE

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.
Packaging image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts

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.
if swallowed, get medical help or contact a Poison Control Center right away.

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: Flamable, keep away from fire or flame or sparks. For external use only When using this product do not use in or near eyes If case of contact, rinse eyes thoroughly with water Stop use and ask a doctor if Irritation or rash appears on the skin.

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