NDC 71578-001 Hair Regenerator
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71578 - Nuggela & Sule Sl
- 71578-001 - Hair Regenerator
Product Packages
NDC Code 71578-001-02
Package Description: 1 AMPULE in 1 BOX / 10 mL in 1 AMPULE (71578-001-01)
Product Details
What is NDC 71578-001?
What are the uses for Hair Regenerator?
Which are Hair Regenerator UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Hair Regenerator 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:
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- BIOTIN (UNII: 6SO6U10H04)
- LINALOOL, (-)- (UNII: 3U21E3V8I2)
- WATER (UNII: 059QF0KO0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROLYZED PLACENTAL PROTEIN (BOVINE) (UNII: KR5CS6RBH9)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- SOY PROTEIN (UNII: R44IWB3RN5)
- PROPANEDIOL (UNII: 5965N8W85T)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCOGEN (UNII: 309GSC92U1)
- POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- DEXTROSE (UNII: IY9XDZ35W2)
- PHENYLPROPANOL (UNII: 0F897O3O4M)
- ORNITHINE HYDROCHLORIDE (UNII: HBK84K66XH)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PANTHENOL (UNII: WV9CM0O67Z)
- LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- CITRULLINE (UNII: 29VT07BGDA)
- SODIUM SUCCINATE HEXAHYDRATE (UNII: U16QOD6C4E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SORBIC ACID (UNII: X045WJ989B)
- ALCOHOL (UNII: 3K9958V90M)
* 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".