NDC 55118-580 Kleenex Antiseptic Hand Rub With Moisturizers
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 55118-580?
What are the uses for Kleenex Antiseptic Hand Rub With Moisturizers?
Which are Kleenex Antiseptic Hand Rub With Moisturizers UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Kleenex Antiseptic Hand Rub With Moisturizers Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- CETETH-10 (UNII: LF9X1PN3XJ)
- STEARETH-21 (UNII: 53J3F32P58)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLOXAMER 335 (UNII: G6DQL26D50)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Kleenex Antiseptic Hand Rub With Moisturizers?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".