NDC 24909-162 Terrasil Rapid-relief Vaginal
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What is NDC 24909-162?
What are the uses for Terrasil Rapid-relief Vaginal?
Which are Terrasil Rapid-relief Vaginal UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
Which are Terrasil Rapid-relief Vaginal 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:
- BENTONITE (UNII: A3N5ZCN45C)
- JOJOBA OIL (UNII: 724GKU717M)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SAGE OIL (UNII: U27K0H1H2O)
- SILVER OXIDE (UNII: 897WUN6G6T)
- TEA TREE OIL (UNII: VIF565UC2G)
- WHITE WAX (UNII: 7G1J5DA97F)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURIC ACID (UNII: 1160N9NU9U)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PALM ACID (UNII: B6G0Y5Z616)
- PALM KERNEL ACID (UNII: 79P21R4317)
- PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SHEA BUTTER (UNII: K49155WL9Y)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM PALMATE (UNII: S0A6004K3Z)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- SORBITOL (UNII: 506T60A25R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Terrasil Rapid-relief Vaginal?
- RxCUI: 1535160 - miconazole nitrate 2 % Vaginal Ointment
- RxCUI: 1535160 - miconazole nitrate 0.02 MG/MG Vaginal Ointment
- RxCUI: 1535168 - miconazole nitrate 2 % Medicated Bar Soap
- RxCUI: 1535168 - miconazole nitrate 0.02 MG/MG Medicated Bar Soap
- RxCUI: 1535503 - {1 (75000 MG) (miconazole nitrate 0.02 MG/MG Medicated Bar Soap) / 1 (25000 MG) (miconazole nitrate 0.02 MG/MG Vaginal Ointment) } Pack
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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".