NDC 71157-0020 Rough Dry
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71157-0020?
What are the uses for Rough Dry?
Which are Rough Dry 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 Rough Dry 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:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- WHITE WAX (UNII: 7G1J5DA97F)
- COCOA BUTTER (UNII: 512OYT1CRR)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- PATCHOULI OIL (UNII: F3IN55X5PO)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- ALMOND (UNII: 3Z252A2K9G)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- HYDROGENATED MACADAMIA SEED OIL (UNII: W4FFC8IM2K)
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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".