NDC 58443-0065 Panama Jack Spf 4
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises, Inc.
- 58443-0065 - Panama Jack
Product Characteristics
Product Packages
NDC Code 58443-0065-4
Package Description: 177 mL in 1 BOTTLE
Product Details
What is NDC 58443-0065?
What are the uses for Panama Jack Spf 4?
Which are Panama Jack Spf 4 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Panama Jack Spf 4 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:
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- UBIDECARENONE (UNII: EJ27X76M46)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".