NDC 62558-001 Doctor Manzanilla Cough Suppressant And Nasal Decongestant
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62558-001?
What are the uses for Doctor Manzanilla Cough Suppressant And Nasal Decongestant?
Which are Doctor Manzanilla Cough Suppressant And Nasal Decongestant UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Doctor Manzanilla Cough Suppressant And Nasal Decongestant 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Doctor Manzanilla Cough Suppressant And Nasal Decongestant?
- RxCUI: 1086720 - diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG in 5 mL Oral Solution
- RxCUI: 1086720 - diphenhydramine hydrochloride 2.5 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
- RxCUI: 1086720 - diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG per 5 ML Oral 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".