NDC 49520-502 Calm It Down Kit
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49520-502?
What are the uses for Calm It Down Kit?
Which are Calm It Down Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Calm It Down Kit 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- CALCIUM BEHENATE (UNII: J5VFA9V6YG)
- MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- LYCOPENE (UNII: SB0N2N0WV6)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUCROSE PALMITATE (UNII: 3OSQ643ZK5)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
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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".