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  4. NDC Product Code: 69779-012 Sleep

NDC 69779-012 Sleep

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69779-012?
  4. Sleep 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:
69779-012
Proprietary Name:
Sleep
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
dc353895-3a58-475c-8afd-ab08b27b96c3
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 69779-012?

The NDC code 69779-012 is assigned by the FDA to the product Sleep which is product labeled by Siddha Flower Essences Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69779-012-01 1 bottle in 1 carton / 29.6 ml in 1 bottle, 69779-012-02 1 bottle in 1 carton / 7.5 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 Sleep?

Spray in mouth at bedtimefor maximum effect spray in mouth one hour before bed and again at bedtimecan also be used after waking up in the middle of the nightuse 5 days per week until symptoms are relievedadults and children 12 years and over 4-5 sprays per dose children 2 years to under 12 years 2-3 sprays per dose children under 2 years consult a doctor

Which are Sleep 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)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
  • CARBONATE ION (UNII: 7UJQ5OPE7D) (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)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)

Which are Sleep 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".