NDC 61096-0006 Sprayology Stress Relief

Product Information

Sprayology Stress Relief is product labeled by Eight And Company. The product's dosage form is and is administered via form.

Product Code61096-0006
Proprietary Name 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.
Sprayology Stress Relief
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Eight And Company
Labeler Code61096
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
02-26-2014
Listing Expiration Date 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.
12-31-2018
Exclude Flag 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".
I
NDC Code Structure

What are the uses for Sprayology Stress Relief?


Product Packages

NDC 61096-0006-1

Package Description: 1 BOTTLE, SPRAY in 1 CARTON > 41 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Sprayology Stress Relief Active Ingredients UNII Codes

Sprayology 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.

* Please review the disclaimer below.

Sprayology Stress Relief Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Otc - Active Ingredient



Active Ingredients: Agnus castus 6X, Avena sativa 1X, Cinchona officinalis 6X, Humulus lupulus 2X, Hyoscyamus niger 200C, Ignatia amara 200C, Passiflora incarnata 3X, Valeriana officinalis 3X


Warnings



Warnings: If symptoms persist or worsen, stop use and seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.


Dosage & Administration



Directions:

  • Adults and children over 12: 2 sprays into the mouth each 60 minutes as needed for symptom relief the first day, 2 sprays 3 times a day thereafter.
  • Ages 2 to 12: 1 spray into the mouth each 60 minutes as needed for symptom relief the first day, 1 spray 3 times a day thereafter.
  • Under age 2: consult a health care professional.

Otc - Purpose



Temporarily relieves feelings of stress, including:

  • anxiety
  • nervousness
  • mood swings
  • irritability

Other Safety Information



Other Information: Do not use if the transparent seal around spray bottle is broken or missing.


Inactive Ingredient



Inactive Ingredients: Glycerin 10% v/v, non-GMO organic alcohol 9% v/v and purified water.


Indications & Usage



Temporarily relieves feelings of stress, including:

° anxiety

° nervousness

° mood swings

° irritability

° natural

° gluten free

° no artificial flavors or colors

° no known negative side effects

° no known negative drug interactions


* Please review the disclaimer below.