NDC 69804-004 Yowch For Minor Burns By Pain Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69804 - Ridge Properties
- 69804-004 - Yowch For Minor Burns By Pain Balm
Product Packages
NDC Code 69804-004-02
Package Description: 57600 mg in 1 JAR
NDC Code 69804-004-03
Package Description: 113400 mg in 1 JAR
Product Details
What is NDC 69804-004?
Which are Yowch For Minor Burns By Pain Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Yowch For Minor Burns By Pain Balm 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:
- COCOA BUTTER (UNII: 512OYT1CRR)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- NUTMEG OIL (UNII: Z1CLM48948)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- MANGO SEED OIL (UNII: K8LOR30915)
- WITCH HAZEL (UNII: 101I4J0U34)
- WALNUT OIL (UNII: Y0P3555R51)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- MORINGA OLEIFERA SEED OIL (UNII: REM6A5QMC0)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)
- COCONUT OIL (UNII: Q9L0O73W7L)
What is the NDC to RxNorm Crosswalk for Yowch For Minor Burns By Pain Balm?
- RxCUI: 1432482 - lidocaine HCl 2 % Topical Cream
- RxCUI: 1432482 - lidocaine hydrochloride 20 MG/ML Topical Cream
- RxCUI: 1432482 - lidocaine hydrochloride 2 % Topical Cream
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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".