NDC 17312-175 Ring Relief Pm Nighttime Formula
Arnica Montana,Calcium Sulfide,Hypericum Perforatum,Lycopodium Clavatum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17312 - Trp Company
- 17312-175 - Ring Relief Pm Nighttime Formula
Product Packages
NDC Code 17312-175-15
Package Description: 1 BOTTLE, DROPPER in 1 PACKAGE / 10 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17312-175?
What are the uses for Ring Relief Pm Nighttime Formula?
What are Ring Relief Pm Nighttime Formula Active Ingredients?
- ALLYLTHIOUREA 6 [hp_X]/mL
- ARNICA MONTANA 6 [hp_X]/mL
- CALCIUM SULFIDE 13 [hp_X]/mL
- HYPERICUM PERFORATUM 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MATRICARIA CHAMOMILLA 12 [hp_X]/mL
- PASSIFLORA INCARNATA FLOWER 5 [hp_X]/mL
- SALICYLIC ACID 6 [hp_X]/mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
- SILICON DIOXIDE 13 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- VALERIAN 6 [hp_X]/mL - A plant genus of the family VALERIANACEAE, order Dipsacales, subclass Asteridae, class Magnoliopsida. It is best known for the sedative use and valepotriate content of the roots. It is sometimes called Garden Heliotrope but is unrelated to true Heliotrope (HELIOTROPIUM).
Which are Ring Relief Pm Nighttime Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)
- PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z) (Active Moiety)
- ALLYLTHIOUREA (UNII: 706IDJ14B7)
- ALLYLTHIOUREA (UNII: 706IDJ14B7) (Active Moiety)
Which are Ring Relief Pm Nighttime Formula 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
* 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".