NDC 68678-065 Protec Pain Relief Cold Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68678 - Ahc Ventures
- 68678-065 - Protec Pain Relief Cold Therapy
Product Characteristics
Product Packages
NDC Code 68678-065-04
Package Description: 126 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 68678-065?
What are the uses for Protec Pain Relief Cold Therapy?
Which are Protec Pain Relief Cold Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Protec Pain Relief Cold Therapy 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:
- ALCOHOL (UNII: 3K9958V90M)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- HYALURONIC ACID (UNII: S270N0TRQY)
- ARNICA MONTANA (UNII: O80TY208ZW)
- BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
- YUCCA SCHIDIGERA (UNII: 08A0YG3VIC)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- WATER (UNII: 059QF0KO0R)
- NITRIC OXIDE (UNII: 31C4KY9ESH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Protec Pain Relief Cold Therapy?
- RxCUI: 351286 - menthol 8 % Topical Spray
- RxCUI: 351286 - menthol 80 MG/ML Topical Spray
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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".