NDC 59667-0088 Nighty Night

Argentum 30c, Arsenicum 30c, Belladonna 30c, Calc Phos 30c, Chelidonium 30c, Coffea 30c, Lillium 30c, Podophyllum 30c Pulsatilla 30c, Rhus Tox 30c

NDC Product Code 59667-0088

NDC Code: 59667-0088

Proprietary Name: Nighty Night What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Argentum 30c, Arsenicum 30c, Belladonna 30c, Calc Phos 30c, Chelidonium 30c, Coffea 30c, Lillium 30c, Podophyllum 30c Pulsatilla 30c, Rhus Tox 30c 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.

NDC Code Structure

  • 59667 - Home Sweet Homeopathics
    • 59667-0088 - Nighty Night

NDC 59667-0088-2

Package Description: 30 [hp_C] in 1 BOTTLE, SPRAY

NDC Product Information

Nighty Night with NDC 59667-0088 is a a human over the counter drug product labeled by Home Sweet Homeopathics. The generic name of Nighty Night is argentum 30c, arsenicum 30c, belladonna 30c, calc phos 30c, chelidonium 30c, coffea 30c, lillium 30c, podophyllum 30c pulsatilla 30c, rhus tox 30c. The product's dosage form is spray and is administered via oral form.

Labeler Name: Home Sweet Homeopathics

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Nighty Night Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SILVER NITRATE 30 [hp_C]/30[hp_C]
  • ARSENIC TRIOXIDE 30 [hp_C]/30[hp_C]
  • ATROPA BELLADONNA 30 [hp_C]/30[hp_C]
  • TRIBASIC CALCIUM PHOSPHATE 30 [hp_C]/30[hp_C]
  • CHELIDONIUM MAJUS 30 [hp_C]/30[hp_C]
  • ARABICA COFFEE BEAN 30 [hp_C]/30[hp_C]
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 30 [hp_C]/30[hp_C]
  • PODOPHYLLUM 30 [hp_C]/30[hp_C]
  • PULSATILLA VULGARIS 30 [hp_C]/30[hp_C]
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/30[hp_C]

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Home Sweet Homeopathics
Labeler Code: 59667
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 08-02-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: E 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Nighty Night Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Purpose

For symptoms associated with

Indications & Usage

To be used according to label indications.

Directions:

Spritz 1 time under the tongue 3 x per day until improvement is seen, dose once each time symptoms return.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

If no improvement is seen after 7 days or new symptoms develop, discontinue use.

Active Ingredients:

Listed for each remedy.

Inactive Ingredients:

In reverse osmosis water with less than 1% alcohol.

* Please review the disclaimer below.

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