NDC 50090-4640 Neptune Ice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4640 - Neptune Ice
Product Packages
NDC Code 50090-4640-0
Package Description: 89 mL in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 50090-4640?
What are the uses for Neptune Ice?
Which are Neptune Ice UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Neptune Ice 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- INDIAN FRANKINCENSE OIL (UNII: 5T1XCE6K8K)
- WATER (UNII: 059QF0KO0R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- ALCOHOL (UNII: 3K9958V90M)
- TROLAMINE (UNII: 9O3K93S3TK)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Neptune Ice?
- RxCUI: 2186001 - camphor 3 % / dimethicone 3 % / lidocaine 4 % / menthol 1 % Topical Gel
- RxCUI: 2186001 - camphor 0.03 MG/MG / dimethicone 0.03 MG/MG / lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Topical Gel
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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".