NDC 13630-0090 Occulus Skin Hydrating Topical Foam Clo-1 Antifungal Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging, Inc.
- 13630-0090 - Occulus
Product Characteristics
Product Packages
NDC Code 13630-0090-3
Package Description: 125 g in 1 CAN
Product Details
What is NDC 13630-0090?
What are the uses for Occulus Skin Hydrating Topical Foam Clo-1 Antifungal Foam?
Which are Occulus Skin Hydrating Topical Foam Clo-1 Antifungal Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Occulus Skin Hydrating Topical Foam Clo-1 Antifungal Foam 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:
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- PALMITIC ACID (UNII: 2V16EO95H1)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POVIDONES (UNII: FZ989GH94E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- UBIDECARENONE (UNII: EJ27X76M46)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Occulus Skin Hydrating Topical Foam Clo-1 Antifungal Foam?
- RxCUI: 1299969 - clotrimazole 1 % Topical Foam
- RxCUI: 1299969 - clotrimazole 10 MG/ML Topical Foam
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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".