NDC 55319-432 Hand Sanitizer With Moisturizers And Aloe Vera Modesa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55319 - Family Dollar Services Inc.
- 55319-432 - Hand Sanitizer With Moisturizers And Aloe Vera
Product Packages
NDC Code 55319-432-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 55319-432-08
Package Description: 237 mL in 1 BOTTLE, PUMP
NDC Code 55319-432-33
Package Description: 1000 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 55319-432?
What are the uses for Hand Sanitizer With Moisturizers And Aloe Vera Modesa?
Which are Hand Sanitizer With Moisturizers And Aloe Vera Modesa 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 Aloe Vera Modesa 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer With Moisturizers And Aloe Vera Modesa?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
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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".