NDC 60611-0110 Edenhills Umjizzang Multi Cleaner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60611 - C&bcosmetic Co., Ltd.
- 60611-0110 - Edenhills Umjizzang Multi Cleaner
Product Packages
NDC Code 60611-0110-1
Package Description: 100 mL in 1 CARTON
Product Details
What is NDC 60611-0110?
What are the uses for Edenhills Umjizzang Multi Cleaner?
Which are Edenhills Umjizzang Multi Cleaner UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Edenhills Umjizzang Multi Cleaner 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:
- CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- USNEA BARBATA (UNII: D6DVA9TCAP)
- PULSATILLA CERNUA ROOT (UNII: FY35I16MPL)
- SCIADOPITYS VERTICILLATA ROOT (UNII: 4BXP7G02TJ)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- NELUMBO NUCIFERA SEED (UNII: YCT65RT6AE)
- CITRUS JUNOS FRUIT (UNII: 53KHW58C1V)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- ZINC SULFATE, UNSPECIFIED FORM (UNII: 89DS0H96TB)
- BETAINE (UNII: 3SCV180C9W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- WATER (UNII: 059QF0KO0R)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* 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".