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Soft care instant hand sanitizer af - Medication Information

Product NDC Code 64536-3628
Drug Name

Soft care instant hand sanitizer af

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1049254
Application Number part333A
Labeler Name Diversey, Inc.
Packages
Package NDC Code Description
64536-3628-3 1300 ml in 1 bottle, pump (64536-3628-3)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzalkonium Chloride 0.13%

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: Apply 0.4-1 ml into hands. Rub product vigorously over hands covering all surfaces. Allow to air dry - do not rinse.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Water, Cocamidopropyl betaine, Propylene glycol, Phenoxyethanol, PEG-7 Glyceryl cocoate, Fragrance, Tetrasodium EDTA, Aloe barbadensis leaf juice, Tocopheryl acetate

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: For hands to decrease bacteria on the skin. Recommended for repeated use.

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.
Soft Care Instant Hand Sanitizer AF BENZALKONIUM CHLORIDE WATER COCAMIDOPROPYL BETAINE PROPYLENE GLYCOL PHENOXYETHANOL PEG-7 GLYCERYL COCOATE EDETATE SODIUM ALOE VERA LEAF .ALPHA.-TOCOPHEROL ACETATE BENZALKONIUM CHLORIDE BENZALKONIUM

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.
NDC 64536-3628-3 Diversey SoftCare Instant Hand Sanitizer AF Alcohol-Free Foam Hand Sanitizer (L) Exp. NSF Nonfood Compounds Program Listed E3 Registration # 156292 Net Contents 1.3 L/ 1.37 U.S. Qt, SKU: 100961733 container label DSCIHAAFDL2f container label DSCIHAAFDL2b

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 in the eyes.

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. Do not use if you are allergic to any ingredients.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-800-558-2332 Monday through Friday 7:30 AM to 5:00 PM Central Standard Time www.sealedair.com

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 and redness develop. If condition persists for more than 72 hours consult a doctor.

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 get into the eyes. In case of contact, immediately flush with water.

References

This field may contain references when prescription drug labeling must summarize or otherwise relay on a recommendation by an authoritative scientific body, or on a standardized methodology, scale, or technique, because the information is important to prescribing decisions.
Other information: EMERGENCY PHONE: 1-800-851-7145 See SDS MS0881162 FOR COMMERCIAL USE See container for Lot Code and Expiry Date. Store in a cool dry place.

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. Do not ingest Do not use in the eyes. When using this product do not get into the eyes. In case of contact, immediately flush with water. Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use if you are allergic to any ingredients.

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