NDC 44781-190 Rebirth Hair Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44781 - Zion Synthetic Fiber Co., Ltd.
- 44781-190 - Rebirth Hair Tonic
Product Packages
NDC Code 44781-190-01
Package Description: 130 mL in 1 CARTON
Product Details
What is NDC 44781-190?
What are the uses for Rebirth Hair Tonic?
Which are Rebirth Hair Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- WITCH HAZEL (UNII: 101I4J0U34)
- WITCH HAZEL (UNII: 101I4J0U34) (Active Moiety)
Which are Rebirth Hair Tonic 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)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PANTHENOL (UNII: WV9CM0O67Z)
- MENTHOL (UNII: L7T10EIP3A)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- PURSLANE (UNII: M6S840WXG5)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- SESAME OIL (UNII: QX10HYY4QV)
- SOYBEAN (UNII: L7HT8F1ZOD)
- MORUS ALBA POLLEN (UNII: 3I9T68187H)
- ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
- POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".