NDC 49980-001 Zhenweilong Huoluo You External Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49980 - Hong Kong Zihua Pharmaceutical Ltd.
- 49980-001 - Zhenweilong Huoluo You
Product Packages
NDC Code 49980-001-01
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS (49980-001-50)
Product Details
What is NDC 49980-001?
What are the uses for Zhenweilong Huoluo You External Analgesic?
Which are Zhenweilong Huoluo You External Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Zhenweilong Huoluo You External Analgesic 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:
- DRAGON'S BLOOD (UNII: M3YJ2C28IC)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEPPERMINT OIL (UNII: AV092KU4JH)
What is the NDC to RxNorm Crosswalk for Zhenweilong Huoluo You External Analgesic?
- RxCUI: 1435162 - camphor 10 % / menthol 15 % / methyl salicylate 30 % Topical Oil
- RxCUI: 1435162 - camphor 100 MG/ML / menthol 150 MG/ML / methyl salicylate 300 MG/ML Topical Oil
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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".