NDC 55319-503 Hand Sanitizer With Moisturizers And Vitamin E
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55319 - Family Dollar Services Inc.
- 55319-503 - Hand Sanitizer
Product Packages
NDC Code 55319-503-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 55319-503-08
Package Description: 237 mL in 1 BOTTLE, PUMP
NDC Code 55319-503-10
Package Description: 295 mL in 1 BOTTLE, PUMP
NDC Code 55319-503-17
Package Description: 3 BOTTLE, PLASTIC in 1 BLISTER PACK / 59 mL in 1 BOTTLE, PLASTIC (55319-503-01)
NDC Code 55319-503-33
Package Description: 1000 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 55319-503?
What are the uses for Hand Sanitizer With Moisturizers And Vitamin E?
Which are Hand Sanitizer With Moisturizers And Vitamin E UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer With Moisturizers And Vitamin E 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:
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer With Moisturizers And Vitamin E?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* 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".