NDC 70994-605 Sportsman Goo
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70994-605?
What are the uses for Sportsman Goo?
Which are Sportsman Goo 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)
- ST. JOHN'S WORT (UNII: UFH8805FKA)
- ST. JOHN'S WORT (UNII: UFH8805FKA) (Active Moiety)
- STELLARIA MEDIA (UNII: 2H03479QVR)
- STELLARIA MEDIA (UNII: 2H03479QVR) (Active Moiety)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7)
- COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7) (Active Moiety)
- SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E)
- SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E) (Active Moiety)
- COMFREY LEAF (UNII: DG4F8T839X)
- COMFREY LEAF (UNII: DG4F8T839X) (Active Moiety)
Which are Sportsman Goo 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- STYRAX BENZOIN RESIN (UNII: FE663Z8IRO)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- OLIVE OIL (UNII: 6UYK2W1W1E)
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[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".