NDC 44781-120 Wrinkless Plus Ct-1 Lifting Up Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44781 - Zion Synthetic Fiber Co., Ltd.
- 44781-120 - Wrinkless Plus
Product Packages
NDC Code 44781-120-01
Package Description: 45 mL in 1 CARTON
Product Details
What is NDC 44781-120?
What are the uses for Wrinkless Plus Ct-1 Lifting Up Essence?
Which are Wrinkless Plus Ct-1 Lifting Up Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Wrinkless Plus Ct-1 Lifting Up Essence 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SOYBEAN OIL (UNII: 241ATL177A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- TOMATO (UNII: Z4KHF2C175)
- WINE GRAPE (UNII: 3GOV20705G)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALUMINUM SILICATE (UNII: T1FAD4SS2M)
- UBIDECARENONE (UNII: EJ27X76M46)
- CARBOMER 934 (UNII: Z135WT9208)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALLANTOIN (UNII: 344S277G0Z)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- POTATO (UNII: CFE1S8DYWD)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
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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".