NDC 43447-9440 Booty Goo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43447 - Skin Sake, Llc
- 43447-9440 - Booty Goo
Product Packages
NDC Code 43447-9440-0
Package Description: 100 PACKET in 1 BOX / 2 g in 1 PACKET (43447-9440-2)
NDC Code 43447-9440-1
Package Description: 71 g in 1 TUBE
Product Details
What is NDC 43447-9440?
What are the uses for Booty Goo?
Which are Booty Goo 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 Booty Goo 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:
- BALSAM PERU (UNII: 8P5F881OCY)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ALOE (UNII: V5VD430YW9)
- BORIC ACID (UNII: R57ZHV85D4)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- CASTOR OIL (UNII: D5340Y2I9G)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- WHITE WAX (UNII: 7G1J5DA97F)
What is the NDC to RxNorm Crosswalk for Booty Goo?
- RxCUI: 1421552 - Booty Goo 25 % Topical Ointment
- RxCUI: 1421552 - zinc oxide 0.25 MG/MG Topical Ointment [Booty Goo]
- RxCUI: 1421552 - Booty Goo 0.25 MG/MG Topical Ointment
- RxCUI: 1421552 - Booty Goo 25 % Ointment
- RxCUI: 1421552 - ZNO 0.25 MG/MG Topical Ointment [Booty Goo]
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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".