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  4. NDC Product Code: 69779-019 Stress Relief

NDC 69779-019 Stress Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69779-019?
  4. Stress Relief 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:
69779-019
Proprietary Name:
Stress Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
99b0dd0a-7d19-448f-8695-b55921036a0e
Start Marketing Date: [9]
04-09-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69779-019?

The NDC code 69779-019 is assigned by the FDA to the product Stress Relief which is product labeled by Siddha Flower Essences Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69779-019-01 1 bottle in 1 carton / 29.6 ml in 1 bottle. 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 Stress Relief?

Children 6 years and older 4 sprays in mouth twice per day 5 days a week children 2 years to under 6 years 2 sprays in mouth only as needed children under 2 years consult a doctor use until symptoms are relievedmay also be applied externally to the top of the child's head

Which are Stress Relief UNII Codes?

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

  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
  • POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
  • POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
  • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ)
  • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ) (Active Moiety)

Which are Stress 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:

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Product Footnotes

[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".