NDC 51393-5004 Stress Less
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51393 - Forces Of Nature
- 51393-5004 - Stress Less
Product Packages
NDC Code 51393-5004-1
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 10 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51393-5004?
What are the uses for Stress Less?
Which are Stress Less UNII Codes?
The UNII codes for the active ingredients in this product are:
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- AVENA SATIVA TOP (UNII: 1ZX4OXU3N6)
- AVENA SATIVA TOP (UNII: 1ZX4OXU3N6) (Active Moiety)
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN)
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
- HOLY BASIL LEAF (UNII: SCJ765569P)
- HOLY BASIL LEAF (UNII: SCJ765569P) (Active Moiety)
- PASSIFLORA EDULIS FLOWER (UNII: SY49TH8VUA)
- PASSIFLORA EDULIS FLOWER (UNII: SY49TH8VUA) (Active Moiety)
- SCUTELLARIA LATERIFLORA (UNII: 7BP4DH5PDC)
- SCUTELLARIA LATERIFLORA (UNII: 7BP4DH5PDC) (Active Moiety)
- VERBENA HASTATA TOP (UNII: CMJ753697I)
- VERBENA HASTATA TOP (UNII: CMJ753697I) (Active Moiety)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
- MACROPIPER METHYSTICUM ROOT (UNII: BOW48C81XP) (Active Moiety)
Which are Stress Less 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
* Please review the disclaimer below.
[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".