NDC 69779-026 Grief And Loss
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69779 - Siddha Flower Essences Llc
- 69779-026 - Grief And Loss
Product Packages
NDC Code 69779-026-01
Package Description: 1 BOTTLE in 1 CARTON / 29.6 mL in 1 BOTTLE
Product Details
What is NDC 69779-026?
What are the uses for Grief And Loss?
Which are Grief And Loss UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
- CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
Which are Grief And Loss 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:
- ARTICHOKE (UNII: 4F3W47PLBE)
- BANANA (UNII: 4AJZ4765R9)
- BITTERSWEET, UNSPECIFIED (UNII: K4QR93EG7I)
- LAMPROCAPNOS SPECTABILIS FLOWER (UNII: X4GD45IWN4)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- WATER (UNII: 059QF0KO0R)
- MORUS RUBRA WHOLE (UNII: NIJ0Z7376A)
* 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".