NDC 14783-400 Lbel Hydra Calme Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd.
- 14783-400 - Lbel
Product Packages
NDC Code 14783-400-02
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE (14783-400-01)
NDC Code 14783-400-04
Package Description: 1 TUBE in 1 BOX / 5 mL in 1 TUBE (14783-400-03)
NDC Code 14783-400-05
Package Description: 1 mL in 1 PACKET
Product Details
What is NDC 14783-400?
What are the uses for Lbel Hydra Calme Spf 15?
Which are Lbel Hydra Calme Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Hydra Calme Spf 15 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PEA (UNII: W4X7H8GYFM)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ERYTHRITOL (UNII: RA96B954X6)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- C20-22 ALCOHOLS (UNII: O4M0347C6A)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLPARABEN (UNII: 14255EXE39)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- RUBUS CHAMAEMORUS FRUIT (UNII: 74CW8G72Q6)
* 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".