NDC 63645-160 Chapice Camphor Phenol Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63645 - Oralabs
- 63645-160 - Chapice Camphor Phenol Gel
Product Characteristics
Product Packages
NDC Code 63645-160-04
Package Description: 1 g in 1 CONTAINER
Product Details
What is NDC 63645-160?
What are the uses for Chapice Camphor Phenol Gel?
Which are Chapice Camphor Phenol Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
Which are Chapice Camphor Phenol Gel 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:
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERIN (UNII: PDC6A3C0OX)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
What is the NDC to RxNorm Crosswalk for Chapice Camphor Phenol Gel?
- RxCUI: 1432785 - Chap Ice with Phenol 10.8 % / 4.7 % Topical Gel
- RxCUI: 1432785 - camphor 0.108 MG/MG / phenol 0.047 MG/MG Topical Gel [ChapIce with Phenol]
- RxCUI: 1432785 - ChapIce with Phenol (camphor 10.8 % / phenol 4.7 % ) Topical Gel
- RxCUI: 308939 - camphor 10.8 % / phenol 4.7 % Topical Gel
- RxCUI: 308939 - camphor 0.108 MG/MG / phenol 0.047 MG/MG Topical Gel
* Please review the disclaimer below.
[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".