NDC 68647-181 Sweat-less
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68647-181?
What are the uses for Sweat-less?
Which are Sweat-less UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- HOPS (UNII: 01G73H6H83)
- HOPS (UNII: 01G73H6H83) (Active Moiety)
- BOWFIN (UNII: HSG9BX3SIJ)
- BOWFIN (UNII: HSG9BX3SIJ) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- CALIFORNIA SHEEPHEAD (UNII: KO849VNU6B)
- CALIFORNIA SHEEPHEAD (UNII: KO849VNU6B) (Active Moiety)
Which are Sweat-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:
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- WATER (UNII: 059QF0KO0R)
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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".