NDC 77249-102 Sani Safe Hand Sanitizer

Product Information

Product Packages

NDC 77249-102-01

Package Description: .1 L in 1 BOTTLE

NDC 77249-102-02

Package Description: .2 L in 1 BOTTLE

NDC 77249-102-05

Package Description: .5 L in 1 BOTTLE

NDC 77249-102-45

Package Description: 5 L in 1 CAN

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

Product Details

Sani Safe Hand Sanitizer is product labeled by Atlantic Care Chemicals Private Limited. The product's dosage form is and is administered via form.


What are Sani Safe Hand Sanitizer Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.

  • BOROGLYCERIN (UNII: U3LMU4AN21)
  • WATER (UNII: 059QF0KO0R)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)


* Please review the disclaimer below.

Sani Safe Hand Sanitizer Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Drug Facts




Active Ingredients



Component

Isopropyl alcohol - 72 % (v/v)


Inactive Ingredients



Boro glycerine, Water, Vitamin E


Otc - Keep Out Of Reach Of Children



• Keep out of Reach of Children


Directions



• Place enough product on hands to cover all surfaces. Rub hands together until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.


Other Information



• Store between 15-30°C (59-86F)

• Avoid freezing and excessive heat above 40°C (104F)


* Please review the disclaimer below.