NDC 61096-0006 Sprayology Stress Relief

NDC Product Code 61096-0006

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.

NDC Product Information

Sprayology Stress Relief with NDC 61096-0006 is a product labeled by Eight And Company. The generic name of Sprayology Stress Relief is . The product's dosage form is and is administered via form.

Labeler Name: Eight And Company

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Eight And Company
Labeler Code: 61096
Start Marketing Date: 02-26-2014 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: 12-31-2018 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Sprayology Stress Relief Product Label Images

Sprayology Stress Relief 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 - 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: anxietynervousnessmood swingsirritability

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.