NDC 70994-104 First Aid 4pc Mini Stick Kit
Calendula Flowers Chamomile Flowers Elder Flowers Yarrow Flowers Red Clover Flowers Sage - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70994-104?
What are the uses for First Aid 4pc Mini Stick Kit?
Which are First Aid 4pc Mini Stick Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA)
- ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA) (Active Moiety)
- COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7)
- COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- STELLARIA MEDIA (UNII: 2H03479QVR)
- STELLARIA MEDIA (UNII: 2H03479QVR) (Active Moiety)
- ST. JOHN'S WORT (UNII: UFH8805FKA)
- ST. JOHN'S WORT (UNII: UFH8805FKA) (Active Moiety)
- COMFREY LEAF (UNII: DG4F8T839X)
- COMFREY LEAF (UNII: DG4F8T839X) (Active Moiety)
- SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E)
- SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E) (Active Moiety)
- CHAMOMILE (UNII: FGL3685T2X)
- CHAMOMILE (UNII: FGL3685T2X) (Active Moiety)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- VIOLA TRICOLOR (UNII: 9Q24RAI43V)
- VIOLA TRICOLOR (UNII: 9Q24RAI43V) (Active Moiety)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- ROSA MOSCHATA OIL (UNII: J99W255AWF)
- ROSA MOSCHATA OIL (UNII: J99W255AWF) (Active Moiety)
Which are First Aid 4pc Mini Stick Kit 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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- STYRAX BENZOIN RESIN (UNII: FE663Z8IRO)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- JOJOBA OIL (UNII: 724GKU717M)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- GINGER OIL (UNII: SAS9Z1SVUK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCONUT OIL (UNII: Q9L0O73W7L)
- HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)
* Please review the disclaimer below.
[1] 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.
[3] 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.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[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".