NDC 59779-538 Pinworm Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy Inc.
- 59779-538 - Pinworm Treatment
Product Characteristics
Product Packages
NDC Code 59779-538-02
Package Description: 1 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
Product Details
What is NDC 59779-538?
What are the uses for Pinworm Treatment?
Which are Pinworm Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRANTEL PAMOATE (UNII: 81BK194Z5M)
- PYRANTEL (UNII: 4QIH0N49E7) (Active Moiety)
Which are Pinworm Treatment 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:
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Pinworm Treatment?
- RxCUI: 199106 - pyrantel pamoate 144 MG in 1 mL Oral Suspension
- RxCUI: 199106 - pyrantel pamoate 144 MG/ML Oral Suspension
- RxCUI: 199106 - pyrantel pamoate 144 MG per 1 ML Oral Suspension
- RxCUI: 199106 - pyrantel pamoate 144 MG/ML (pyrantel base 50 MG/ML) Oral Suspension
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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".