NDC 50804-779 Goodsense Diaper Rash
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50804-779?
What are the uses for Goodsense Diaper Rash?
Which are Goodsense Diaper Rash UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Goodsense Diaper Rash 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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PARAFFIN (UNII: I9O0E3H2ZE)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- LANOLIN (UNII: 7EV65EAW6H)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- SQUALANE (UNII: GW89575KF9)
- TALC (UNII: 7SEV7J4R1U)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
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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".