NDC 64536-7291 Soft Care Foam Instant Hand Sanitizer

NDC Product Code 64536-7291

NDC 64536-7291-1

Package Description: 1 L in 1 BAG

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Soft Care Foam Instant Hand Sanitizer with NDC 64536-7291 is a product labeled by Diversey, Inc.. The generic name of Soft Care Foam Instant Hand Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Diversey, Inc.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Diversey, Inc.
Labeler Code: 64536
Start Marketing Date: 08-02-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Soft Care Foam Instant Hand Sanitizer Product Label Images

Soft Care Foam Instant Hand Sanitizer Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active ingredientEthyl alcohol 62% v/v

Otc - Purpose


Indications & Usage

UsesTo decrease bacteria on hands.


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

Otc - When Using

When using this product.Do not use in the eyes.In case of contact, immediately flush with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develop.If condition persists for more than 72 hours, consult a doctor.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

DirectionsApply 1-2 ml into hands, rub product vigorously over hands covering all surfaces.Allow to air dry.


Other informationEMERGENCY PHONE: 1-800-851-7145See SDS MS0301383Store below 35 C (95 F)See container for Lot Code and Expiry DateDo not contaminate water, food or feed during use, storage or disposal.For Commercial and Industrial Use Only

Inactive Ingredient

Inactive ingredientsWater, PEG-10 Dimethicone, Glycerin, Isopropyl Myristate, polyquaternium-11, Disodium EDTA, Aloe Barbabensis Leaf Juice, Tocopheryl Acetate

Otc - Questions

Questions or comments?1-800-558-2332 Monday through Friday 7:30 AM to 5:00 PM Central Standard Timewww.diversey.com

* Please review the disclaimer below.