NDC 69008-4010 Combination Remedy 10 - Menstrual Pain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69008 - Warsan Homoeopathic Laboratories
- 69008-4010 - Combination Remedy 10 - Menstrual Pain
Product Packages
NDC Code 69008-4010-1
Package Description: 20 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 69008-4010?
What are the uses for Combination Remedy 10 - Menstrual Pain?
Which are Combination Remedy 10 - Menstrual Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- SAFFRON (UNII: E849G4X5YJ)
- SAFFRON (UNII: E849G4X5YJ) (Active Moiety)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
Which are Combination Remedy 10 - Menstrual Pain 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".