NDC 50563-340 Body Prescriptions Pink Peony Infused With Vitamin E Antibacterial Hand
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What is NDC 50563-340?
What are the uses for Body Prescriptions Pink Peony Infused With Vitamin E Antibacterial Hand?
Which are Body Prescriptions Pink Peony Infused With Vitamin E Antibacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Body Prescriptions Pink Peony Infused With Vitamin E Antibacterial Hand 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Body Prescriptions Pink Peony Infused With Vitamin E Antibacterial Hand?
- RxCUI: 1046442 - benzalkonium chloride 0.13 % Topical Lotion
- RxCUI: 1046442 - benzalkonium chloride 1.3 MG/ML Topical Lotion
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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".