NDC 61727-054 Menopause Relief Homeopathic Remedy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61727 - Homeocare Laboratories Inc.
- 61727-054 - Menopause Relief Homeopathic Remedy
Product Packages
NDC Code 61727-054-02
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 61727-054?
What are the uses for Menopause Relief Homeopathic Remedy?
Which are Menopause Relief Homeopathic Remedy UNII Codes?
The UNII codes for the active ingredients in this product are:
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- LACHESIS MUTA WHOLE (UNII: 6Y582I290C)
- LACHESIS MUTA WHOLE (UNII: 6Y582I290C) (Active Moiety)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8)
- DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (Active Moiety)
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT)
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT) (Active Moiety)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
- SEPIA ESCULENTA WHOLE (UNII: 6ET21QP634)
- SEPIA ESCULENTA WHOLE (UNII: 6ET21QP634) (Active Moiety)
- SUS SCROFA OVARY (UNII: S7YTV04R8O)
- SUS SCROFA OVARY (UNII: S7YTV04R8O) (Active Moiety)
Which are Menopause Relief Homeopathic Remedy 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- 2,4-DIAMINO-5-METHYLPHENOXYETHANOL HYDROCHLORIDE (UNII: Z28JS1XMY2)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POLYETHYLENE OXIDE 1000000 (UNII: HZ58M6D839)
- WATER (UNII: 059QF0KO0R)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIMETHICONE 1000 (UNII: MCU2324216)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CETYL ALCOHOL (UNII: 936JST6JCN)
* 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".