NDC 42979-100 Hes Clean
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42979 - Doctor C&c Co., Ltd.
- 42979-100 - Hes Clean
Product Packages
NDC Code 42979-100-01
Package Description: 200 mL in 1 CARTON
Product Details
What is NDC 42979-100?
What are the uses for Hes Clean?
Which are Hes Clean UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hes Clean 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:
- WATER (UNII: 059QF0KO0R)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- CHENOPODIUM ALBUM FLOWER (UNII: 0W0371JRM3)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- OREGANO (UNII: 0E5AT8T16U)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- PURSLANE (UNII: M6S840WXG5)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- ROSEMARY (UNII: IJ67X351P9)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- BASIL (UNII: 2U0KZP0FDW)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- FENNEL (UNII: 557II4LLC3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
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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".