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Warm vanilla hand sanitizer - Medication Information

Product NDC Code 58503-004
Drug Name

Warm vanilla hand sanitizer

Type Brand
Active Ingredients
Alcohol 147 ml/237ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 581660
Application Number part333E
Labeler Name China Ningbo Shangge Cosmetic Technology Corp.
Packages
Package NDC Code Description
58503-004-01 237 ml in 1 bottle (58503-004-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Purpose Ethyl Alcohol 62.0%...........................Antimicrobial

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 briskly rub hands together until dry supervise children under 6 years in the use of this product

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, fd&c yellow no.5, fd&c red no.33.

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.
Other information store at 20oC to 25oC (68o to 77oF) may discolor certain fabrics

Purpose

Information about the drug product’s indications for use.
Uses for handwashing to decrease the bacteria on the skin recommended for repeated use

Spl product data elements

Usually a list of ingredients in a drug product.
Warm Vanilla Hand Sanitizer Ethyl Alcohol WATER CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) TROLAMINE GLYCERIN PROPYLENE GLYCOL ALOE VERA LEAF D&C RED NO. 33 FD&C YELLOW NO. 5 ALCOHOL ALCOHOL

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 image

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.

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 and flame. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

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