NDC 51439-002 Simply Firm - Face And Neck Non Surgical Face Lift
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51439 - Carepluss Pharma S.a. De C.v.
- 51439-002 - Simply Firm - Face And Neck
Product Packages
NDC Code 51439-002-01
Package Description: .119 mg in 1 TUBE
Product Details
What is NDC 51439-002?
What are the uses for Simply Firm - Face And Neck Non Surgical Face Lift?
Which are Simply Firm - Face And Neck Non Surgical Face Lift UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Simply Firm - Face And Neck Non Surgical Face Lift 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- MINERAL OIL (UNII: T5L8T28FGP)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- DEANOL (UNII: 2N6K9DRA24)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COFFEE BEAN (UNII: JFH385Y744)
- TROLAMINE (UNII: 9O3K93S3TK)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- MINT (UNII: FV98Z8GITP)
- ALMOND (UNII: 3Z252A2K9G)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- COCOA (UNII: D9108TZ9KG)
- EDETIC ACID (UNII: 9G34HU7RV0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- WATER (UNII: 059QF0KO0R)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
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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".