NDC 61727-054 Menopause Relief Homeopathic Remedy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 61727-054 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
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)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".