NDC 52490-201 B4 Antiseptic Hand Sanitizer With Ethyl Alcohol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52490 - Midway Advanced Products, Llc
- 52490-201 - B4 Antiseptic Hand Sanitizer With Ethyl Alcohol
Product Packages
NDC Code 52490-201-10
Package Description: 500 CARTON in 1 CARTON / 1.2 mL in 1 CARTON
Product Details
What is NDC 52490-201?
What are the uses for B4 Antiseptic Hand Sanitizer With Ethyl Alcohol?
Which are B4 Antiseptic Hand Sanitizer With Ethyl Alcohol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are B4 Antiseptic Hand Sanitizer With Ethyl Alcohol 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- DIISOPROPYLAMINE (UNII: BR9JLI40NO)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for B4 Antiseptic Hand Sanitizer With Ethyl Alcohol?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % Topical Gel
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[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".