NDC 18472-175 Blue Ice Fermented Cod Liver Oil Calm Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 18472 - Abs Corporation
- 18472-175 - Blue Ice Fermented Cod Liver Oil Calm Balm
Product Packages
NDC Code 18472-175-01
Package Description: 49.5 g in 1 JAR
Product Details
What is NDC 18472-175?
What are the uses for Blue Ice Fermented Cod Liver Oil Calm Balm?
Which are Blue Ice Fermented Cod Liver Oil Calm Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Blue Ice Fermented Cod Liver Oil Calm Balm 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:
- SHEA BUTTER (UNII: K49155WL9Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- OLEIC ACID (UNII: 2UMI9U37CP)
- WHITE WAX (UNII: 7G1J5DA97F)
- COD LIVER OIL (UNII: BBL281NWFG)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ROSEMARY OIL (UNII: 8LGU7VM393)
What is the NDC to RxNorm Crosswalk for Blue Ice Fermented Cod Liver Oil Calm Balm?
- RxCUI: 1492178 - camphor 2.63 % / eucalyptus oil 3.5 % / menthol 0.74 % Topical Ointment
- RxCUI: 1492178 - camphor 0.0263 MG/MG / Eucalyptus oil 0.035 MG/MG / menthol 0.0074 MG/MG Topical Ointment
* 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".