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  4. NDC Product Code: 70773-103 Rsq Five

NDC 70773-103 Rsq Five

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70773-103?
  4. Rsq Five Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70773-103
Proprietary Name:
Rsq Five
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Private Label Brands Cc
Labeler Code:
70773
Product Label ID:
61566222-27b7-32d2-e053-2a91aa0a11b0
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
12-25-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 70773-103?

The NDC code 70773-103 is assigned by the FDA to the product Rsq Five which is product labeled by Private Label Brands Cc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70773-103-30 1 bottle, dropper in 1 carton / 1 [hp_x] in 1 bottle, dropper. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Rsq Five?

Adults and children:Place 10 drops directly on tongue 3x daily. In severe cases, 10 drops every 15 minutes for an hour, then hourly for 24 hours.Infants:5 - 10 drops diluted in cooled, boiled, water.

Which are Rsq Five UNII Codes?

The UNII codes for the active ingredients in this product are:

  • PHOSPHORIC ACID (UNII: E4GA8884NN)
  • PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
  • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
  • ARNICA MONTANA (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • MELISSA OFFICINALIS (UNII: YF70189L0N)
  • MELISSA OFFICINALIS (UNII: YF70189L0N) (Active Moiety)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS WHOLE (UNII: R0519OZO3K)
  • GELSEMIUM SEMPERVIRENS WHOLE (UNII: R0519OZO3K) (Active Moiety)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
  • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
  • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)

Which are Rsq Five 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:

* Please review the disclaimer below.

Product Footnotes

[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".