NDC 69314-201 Thermal-aid Headache Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69314 - Pacific Shore Holdings, Inc.
- 69314-201 - Thermal-aid
Product Packages
NDC Code 69314-201-42
Package Description: 57 g in 1 TUBE
Product Details
What is NDC 69314-201?
What are the uses for Thermal-aid Headache Relief?
Which are Thermal-aid Headache Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
Which are Thermal-aid Headache Relief 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)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MINERAL OIL (UNII: T5L8T28FGP)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- SOYBEAN OIL (UNII: 241ATL177A)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALMOND OIL (UNII: 66YXD4DKO9)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SQUALENE (UNII: 7QWM220FJH)
- HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)
- GARLIC (UNII: V1V998DC17)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C)
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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".