NDC 76348-605 Restore Lidocaine Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76348-605?
What are the uses for Restore Lidocaine Pain Relief Cream?
Which are Restore Lidocaine Pain Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Restore Lidocaine Pain Relief Cream 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:
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
- WATER (UNII: 059QF0KO0R)
- WHITE WAX (UNII: 7G1J5DA97F)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- JOJOBA OIL (UNII: 724GKU717M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Restore Lidocaine Pain Relief Cream?
- RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 4 % 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".