NDC 0178-0370 Dr. Smiths Rash And Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0178 - Mission Pharmacal Company
- 0178-0370 - Dr. Smiths Rash And Skin
Product Packages
NDC Code 0178-0370-03
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Details
What is NDC 0178-0370?
Which are Dr. Smiths Rash And Skin 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 Dr. Smiths Rash And Skin 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- WATER (UNII: 059QF0KO0R)
- WHITE WAX (UNII: 7G1J5DA97F)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- THYMOL IODIDE (UNII: A51HJM3XSU)
- PARAFFIN (UNII: I9O0E3H2ZE)
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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".