NDC 70611-001 Tropical Pineapple Jumbo Lip Balm
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70611-001?
What are the uses for Tropical Pineapple Jumbo Lip Balm?
Which are Tropical Pineapple Jumbo Lip Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Tropical Pineapple Jumbo Lip Balm 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:
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FERROUS OXIDE (UNII: G7036X8B5H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PODOPHYLLUM RESIN (UNII: 16902YVY2B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SHEA BUTTER (UNII: K49155WL9Y)
- STEVIOSIDE (UNII: 0YON5MXJ9P)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)
- CERESIN (UNII: Q1LS2UJO3A)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- MICA (UNII: V8A1AW0880)
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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".