NDC 45156-5502 Inflammation Otc Bruise Relief
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 45156-5502?
What are the uses for Inflammation Otc Bruise Relief?
Which are Inflammation Otc Bruise Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Inflammation Otc Bruise 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALCOHOL (UNII: 3K9958V90M)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- SOYBEAN OIL (UNII: 241ATL177A)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- LEMON OIL (UNII: I9GRO824LL)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CAT'S CLAW (UNII: 9060PRM18Q)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- WORMWOOD (UNII: F84709P2XV)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARRAGEENAN (UNII: 5C69YCD2YJ)
- GINGER (UNII: C5529G5JPQ)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- UREA (UNII: 8W8T17847W)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- RUSCUS ACULEATUS ROOT (UNII: ZW12V95I1Q)
- BETAINE (UNII: 3SCV180C9W)
- INOSITOL (UNII: 4L6452S749)
- TAURINE (UNII: 1EQV5MLY3D)
- TREHALOSE (UNII: B8WCK70T7I)
- PHYTONADIONE (UNII: A034SE7857)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Inflammation Otc Bruise Relief?
- RxCUI: 1148418 - Inflammation OTC Bruise 3.5 % Topical Lotion
- RxCUI: 1148418 - camphor 35 MG/ML Topical Lotion [Inflammation OTC Bruise]
- RxCUI: 1148418 - Inflammation OTC Bruise 35 MG/ML Topical Lotion
- RxCUI: 435780 - camphor 3.5 % Topical Lotion
- RxCUI: 435780 - camphor 35 MG/ML Topical Lotion
* 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".