NDC 73769-100 Prohemp Soothing Menthol Rub 4%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 73769-100?
What are the uses for Prohemp Soothing Menthol Rub 4%?
Which are Prohemp Soothing Menthol Rub 4% UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Prohemp Soothing Menthol Rub 4% 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .BETA.-CARYOPHYLLENE ALCOHOL (UNII: 9Y50O7OH2E)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- QUILLAJA SAPONARIA BARK (UNII: 8N0K3807ZW)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- HEMP (UNII: TD1MUT01Q7)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
* 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".