NDC 58292-011 On The Go-dose
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58292 - Perfect Measure Llc
- 58292-011 - On The Go-dose
Product Characteristics
Product Packages
NDC Code 58292-011-05
Package Description: 10 VIAL in 1 PACKAGE / 5 mL in 1 VIAL
Product Details
What is NDC 58292-011?
What are the uses for On The Go-dose?
Which are On The Go-dose UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
Which are On The Go-dose 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for On The Go-dose?
- RxCUI: 1049906 - diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
- RxCUI: 1049906 - diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
- RxCUI: 1049906 - diphenhydramine HCl 12.5 MG per 5 ML Oral Solution
- RxCUI: 1049906 - diphenhydramine hydrochloride 25 MG per 10 ML Oral Solution
- RxCUI: 1049906 - diphenhydramine hydrochloride 50 MG per 20 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".