NDC 73272-301 Diclostream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73272 - Upstream Pharma, Llc
- 73272-301 - Diclostream
Product Packages
NDC Code 73272-301-01
Package Description: 1 KIT in 1 CARTON * 150 mL in 1 BOTTLE * 89 mL in 1 BOTTLE
Product Details
What is NDC 73272-301?
What are the uses for Diclostream?
Which are Diclostream UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Diclostream 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:
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- THYMOL (UNII: 3J50XA376E)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Diclostream?
- RxCUI: 1600976 - menthol 10 % Topical Solution
- RxCUI: 1600976 - menthol 100 MG/ML Topical Solution
- RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
- RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
- RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution
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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".