NDC 55946-701 Calendula Diaper Rash Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55946 - Weleda, Inc.
- 55946-701 - Calendula Diaper Rash Cream
Product Packages
NDC Code 55946-701-49
Package Description: 1.5 g in 1 POUCH
NDC Code 55946-701-53
Package Description: 81 g in 1 TUBE
NDC Code 55946-701-54
Package Description: 10.8 g in 1 TUBE
Product Details
What is NDC 55946-701?
What are the uses for Calendula Diaper Rash Cream?
Which are Calendula Diaper Rash Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Calendula Diaper Rash 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CANANGA OIL (UNII: 8YOY78GNNX)
- CHAMOMILE (UNII: FGL3685T2X)
- CITRUS AURANTIUM LEAFY TWIG OIL (UNII: 5K6H1IMT3D)
- CLARY SAGE OIL (UNII: 87L0D4U3M0)
- GLYCERYL MONOLINOLEATE (UNII: 4763AXI84L)
- HECTORITE (UNII: 08X4KI73EZ)
- LANOLIN (UNII: 7EV65EAW6H)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ORANGE OIL (UNII: AKN3KSD11B)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SAGE OIL (UNII: U27K0H1H2O)
- SESAME OIL (UNII: QX10HYY4QV)
- STYRAX BENZOIN RESIN (UNII: FE663Z8IRO)
- ALMOND OIL (UNII: 66YXD4DKO9)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Calendula Diaper Rash Cream?
- RxCUI: 417994 - zinc oxide 12 % Topical Cream
- RxCUI: 417994 - zinc oxide 120 MG/ML Topical Cream
- RxCUI: 417994 - ZNO 120 MG/ML Topical Cream
* 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".