NDC 73862-218 E-pu Premium Mandarin Hand Sanitizing Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73862 - E.cis Cosmetic Co.,ltd
- 73862-218 - E-pu Premium Mandarin Hand Sanitizing Serum
Product Packages
NDC Code 73862-218-12
Package Description: 60 CASE in 1 CARTON / 6 BOTTLE in 1 CASE (73862-218-11) / 100 mL in 1 BOTTLE (73862-218-10)
Product Details
What is NDC 73862-218?
What are the uses for E-pu Premium Mandarin Hand Sanitizing Serum?
Which are E-pu Premium Mandarin Hand Sanitizing Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are E-pu Premium Mandarin Hand Sanitizing Serum 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:
- BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARGAN OIL (UNII: 4V59G5UW9X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ACRYLIC ACID (UNII: J94PBK7X8S)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- WATER (UNII: 059QF0KO0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- MACADAMIA OIL (UNII: 515610SU8C)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PANTHENOL (UNII: WV9CM0O67Z)
- SHEA BUTTER (UNII: K49155WL9Y)
What is the NDC to RxNorm Crosswalk for E-pu Premium Mandarin Hand Sanitizing Serum?
- RxCUI: 637077 - ethanol 62 % Topical Lotion
- RxCUI: 637077 - ethanol 0.62 ML/ML Topical Lotion
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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".