NDC 64539-006 Cicatrix Skin Protectant
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64539-006?
What are the uses for Cicatrix Skin Protectant?
Which are Cicatrix Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Cicatrix Skin Protectant 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:
- COUMARIN (UNII: A4VZ22K1WT)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)
- STEARETH-2 (UNII: V56DFE46J5)
- CERAMIDE 3 (UNII: 4370DF050B)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- CERAMIDE 6 II (UNII: F1X8L2B00J)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- WATER (UNII: 059QF0KO0R)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARETH-20 (UNII: L0Q8IK9E08)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PALMITIC ACID (UNII: 2V16EO95H1)
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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".