NDC 62721-8114 Lornamead Lypsyl
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Product Details
What is NDC 62721-8114?
What are the uses for Lornamead Lypsyl?
Which are Lornamead Lypsyl UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Lornamead Lypsyl 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:
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALLANTOIN (UNII: 344S277G0Z)
- SHEA BUTTER (UNII: K49155WL9Y)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PENTAERYTHRITYL TETRACAPRYLATE/TETRACAPRATE (UNII: 832C4KF14X)
- POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LEVOMENOL (UNII: 24WE03BX2T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- JOJOBA OIL (UNII: 724GKU717M)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CHAMOMILE (UNII: FGL3685T2X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LYSINE (UNII: K3Z4F929H6)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- ZINC LACTATE (UNII: 2GXR25858Y)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
What is the NDC to RxNorm Crosswalk for Lornamead Lypsyl?
- RxCUI: 1421011 - menthol 0.6 % / petrolatum 62 % Paste
- RxCUI: 1421011 - menthol 0.006 MG/MG / petrolatum 0.62 MG/MG Paste
- RxCUI: 1421016 - Lypsyl (menthol 0.6 % / petrolatum 62 % ) Paste
- RxCUI: 1421016 - menthol 0.006 MG/MG / petrolatum 0.62 MG/MG Paste [Lypsyl]
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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".