NDC 73862-226 Hanbee Hand Sanitizer 70% 500ml
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73862 - E.cis Cosmetic Co., Ltd.
- 73862-226 - Hanbee Hand Sanitizer 70% 500ml
Product Packages
NDC Code 73862-226-02
Package Description: 24 BOTTLE, SPRAY in 1 CARTON / 500 mL in 1 BOTTLE, SPRAY (73862-226-01)
Product Details
What is NDC 73862-226?
What are the uses for Hanbee Hand Sanitizer 70% 500ml?
Which are Hanbee Hand Sanitizer 70% 500ml UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hanbee Hand Sanitizer 70% 500ml 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:
- ROYAL JELLY (UNII: L497I37F0C)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HONEY (UNII: Y9H1V576FH)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hanbee Hand Sanitizer 70% 500ml?
- RxCUI: 1041849 - ethanol 70 % Topical Spray
- RxCUI: 1041849 - ethanol 0.7 ML/ML Topical Spray
* 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".