NDC 55249-2001 Tosowoong Mens Booster Repair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55249 - Mantong
- 55249-2001 - Tosowoong Mens Booster Repair
Product Packages
NDC Code 55249-2001-1
Package Description: 150 mL in 1 BOTTLE
Product Details
What is NDC 55249-2001?
What are the uses for Tosowoong Mens Booster Repair?
Which are Tosowoong Mens Booster Repair UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Tosowoong Mens Booster Repair 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)
- ALCOHOL (UNII: 3K9958V90M)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- SQUALENE (UNII: 7QWM220FJH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TREHALOSE (UNII: B8WCK70T7I)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
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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".