NDC 63922-601 999 Ganmaoling Cold
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63922 - Kingsway
- 63922-601 - 999 Ganmaoling
Product Characteristics
Product Packages
NDC Code 63922-601-01
Package Description: 1 BLISTER PACK in 1 BOX / 12 CAPSULE in 1 BLISTER PACK (63922-601-12)
Product Details
What is NDC 63922-601?
What are the uses for 999 Ganmaoling Cold?
Which are 999 Ganmaoling Cold UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are 999 Ganmaoling Cold 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:
- DENDRANTHEMA INDICUM FLOWER (UNII: I6OER6U04L)
- TETRADIUM RUTICARPUM FRUIT (UNII: Q413WWJ3X9)
- ILEX PUBESCENS ROOT (UNII: V5V22LFX73)
- BIDENS BIPINNATA WHOLE (UNII: TRQ4JQ7DJQ)
- PEPPERMINT OIL (UNII: AV092KU4JH)
What is the NDC to RxNorm Crosswalk for 999 Ganmaoling Cold?
- RxCUI: 1303251 - acetaminophen 100 MG / caffeine 2 MG / chlorpheniramine maleate 2 MG Oral Capsule
- RxCUI: 1303251 - APAP 100 MG / Caffeine 2 MG / Chlorpheniramine Maleate 2 MG Oral Capsule
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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".