NDC 53203-101 Herbal Heat
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53203 - Eu Yan Sang (usa) Inc
- 53203-101 - Herbal Heat
Product Packages
NDC Code 53203-101-05
Package Description: 5 PATCH in 1 BOX / 6.7 g in 1 PATCH
Product Details
What is NDC 53203-101?
What are the uses for Herbal Heat?
Which are Herbal Heat 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 Herbal Heat 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:
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- MANDARIN OIL (UNII: NJO720F72R)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
- LANOLIN OIL (UNII: OVV5IIJ58F)
- MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974)
- PINUS MASSONIANA RESIN (UNII: 64S07U83T7)
- RHEUM OFFICINALE STEM (UNII: 82X32CRA5U)
- SESAME OIL (UNII: QX10HYY4QV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- TRICHOSANTHES KIRILOWII ROOT (UNII: V409XGE0TS)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Herbal Heat?
- RxCUI: 1373017 - camphor 1 % / menthol 6 % / methyl salicylate 2 % Medicated Patch
- RxCUI: 1373017 - camphor 0.01 MG/MG / menthol 0.06 MG/MG / methyl salicylate 0.02 MG/MG Medicated Patch
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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".