NDC 70826-576 Hongosan Dsp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 70826-576?
What are the uses for Hongosan Dsp?
Which are Hongosan Dsp UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Hongosan Dsp 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- TEA TREE OIL (UNII: VIF565UC2G)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- MINERAL OIL (UNII: T5L8T28FGP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- STEARAMIDE AMP (UNII: U3K8640346)
- CEDROL (UNII: 63ZM9703BO)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
What is the NDC to RxNorm Crosswalk for Hongosan Dsp?
- RxCUI: 103951 - tolnaftate 1 % Topical Cream
- RxCUI: 103951 - tolnaftate 10 MG/ML Topical Cream
* 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".