NDC 68703-349 Stress Away Anxiety Relief
Aconitum Nap,Alfalfa,Avena,Chamomilla,Gelsemium,Humulus Lupulus,Ignatia,Kali Ars,Kali - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68703 - Silver Star Brands
- 68703-349 - Stress Away Anxiety Relief
Product Packages
NDC Code 68703-349-02
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 68703-349?
What are the uses for Stress Away Anxiety Relief?
What are Stress Away Anxiety Relief Active Ingredients?
- ACONITUM NAPELLUS 10 [hp_X]/59mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
- ALFALFA 10 [hp_X]/59mL
- AVENA SATIVA LEAF 10 [hp_X]/59mL
- DATURA STRAMONIUM 10 [hp_X]/59mL - A plant species of the genus DATURA, family SOLANACEAE, that contains TROPANES and other SOLANACEOUS ALKALOIDS.
- DELPHINIUM STAPHISAGRIA SEED 10 [hp_X]/59mL
- GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/59mL
- HUMULUS LUPULUS WHOLE 10 [hp_X]/59mL
- HYDROCHLORIC ACID 10 [hp_X]/59mL - A strong corrosive acid that is commonly used as a laboratory reagent. It is formed by dissolving hydrogen chloride in water. GASTRIC ACID is the hydrochloric acid component of GASTRIC JUICE.
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL 10 [hp_X]/59mL
- PASSIFLORA INCARNATA FLOWERING TOP 10 [hp_X]/59mL
- PHOSPHORUS P-32 10 [hp_X]/59mL
- POTASSIUM ARSENITE ANHYDROUS 10 [hp_X]/59mL
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM 10 [hp_X]/59mL
- SODIUM PHOSPHATE, DIBASIC 10 [hp_X]/59mL
- STRYCHNOS IGNATII WHOLE 10 [hp_X]/59mL
Which are Stress Away Anxiety Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) (Active Moiety)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- HUMULUS LUPULUS WHOLE (UNII: 912A6Q1N4A)
- HUMULUS LUPULUS WHOLE (UNII: 912A6Q1N4A) (Active Moiety)
- STRYCHNOS IGNATII WHOLE (UNII: 6YSJ329777)
- STRYCHNOS IGNATII WHOLE (UNII: 6YSJ329777) (Active Moiety)
- POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI)
- ARSENITE ION (UNII: N5509X556J) (Active Moiety)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- AVENA SATIVA LEAF (UNII: 206PI19V7R) (Active Moiety)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYDROCHLORIC ACID (UNII: QTT17582CB) (Active Moiety)
- PHOSPHORUS P-32 (UNII: 690284A407)
- PHOSPHORUS P-32 (UNII: 690284A407) (Active Moiety)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- ALFALFA (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
Which are Stress Away Anxiety Relief 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:
- CARYA OVATA BARK (UNII: X765CF609L)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- GLUCOSYL STEVIOL (UNII: TKD5UC898Q)
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY)
Which are the Pharmacologic Classes for Stress Away Anxiety Relief?
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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 ("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".