NDC 69274-003 Vaporizing Chest Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69274 - Four Seasons Trading Inc
- 69274-003 - Vaporizing Chest Rub
Product Packages
NDC Code 69274-003-08
Package Description: 50 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-09
Package Description: 56.6 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-10
Package Description: 100 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-11
Package Description: 113 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-12
Package Description: 150 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-13
Package Description: 170 g in 1 BOTTLE, PLASTIC
NDC Code 69274-003-14
Package Description: 226 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69274-003?
What are the uses for Vaporizing Chest Rub?
Which are Vaporizing Chest Rub 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)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
Which are Vaporizing Chest Rub 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- NUTMEG OIL (UNII: Z1CLM48948)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- THYMOL (UNII: 3J50XA376E)
- CEDAR LEAF OIL (UNII: BJ169U4NLG)
What is the NDC to RxNorm Crosswalk for Vaporizing Chest Rub?
- RxCUI: 1042788 - camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel
- RxCUI: 1042788 - camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 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".