NDC 79426-106 Meli Hands Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 79426-106?
What are the uses for Meli Hands Hand Sanitizer?
Which are Meli Hands Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Meli Hands Hand Sanitizer 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)
- AMYL SALICYLATE (UNII: VZO9C30208)
- AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)
- STAR ANISE OIL (UNII: 6RXP35EIRE)
- BENZYL ACETATE (UNII: 0ECG3V79ZJ)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL BENZOATE (UNII: N863NB338G)
- 3-HEXENYL ACETATE, (3Z)- (UNII: 6INA6GC5I6)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- ELEMI OIL (UNII: RC25F1T45S)
- ETHYL 2-METHYLBUTYRATE (UNII: L1T4AB29DS)
- .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O)
- .GAMMA.-NONALACTONE (UNII: I1XGH66S8P)
- .GAMMA.-OCTALACTONE (UNII: UHD6M52X0K)
- .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)
- GLYCERIN (UNII: PDC6A3C0OX)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- HEXYL ACETATE (UNII: 7U7KU3MWT0)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- MALTOL (UNII: 3A9RD92BS4)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
- 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG)
- SANDALWOOD OIL (UNII: X7X01WMQ5F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- VANILLIN (UNII: CHI530446X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Meli Hands Hand Sanitizer?
- RxCUI: 1041849 - ethanol 70 % Topical Spray
- RxCUI: 1041849 - ethanol 0.7 ML/ML Topical Spray
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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".