NDC 49952-004 Zihua Embrocation Cooling Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49952 - Uncle Bill Trading Usa Inc.
- 49952-004 - Zihua Embrocation
Product Packages
NDC Code 49952-004-01
Package Description: 1 BOTTLE, GLASS in 1 BOX / 26 mL in 1 BOTTLE, GLASS (49952-004-26)
Product Details
What is NDC 49952-004?
What are the uses for Zihua Embrocation Cooling Pain Relief?
Which are Zihua Embrocation Cooling Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Zihua Embrocation Cooling Pain Relief 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:
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Zihua Embrocation Cooling Pain Relief?
- RxCUI: 1495457 - camphor 11 % / menthol 15 % / methyl salicylate 15 % Topical Oil
- RxCUI: 1495457 - camphor 0.11 MG/MG / menthol 0.15 MG/MG / methyl salicylate 0.15 MG/MG 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".