NDC 78902-202 Pearlessence Hand Wash Coconut And Rose
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78902 - Jocott Brands, Inc.
- 78902-202 - Pearlessence Hand Wash
Product Packages
NDC Code 78902-202-16
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 78902-202?
What are the uses for Pearlessence Hand Wash Coconut And Rose?
Which are Pearlessence Hand Wash Coconut And Rose UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Pearlessence Hand Wash Coconut And Rose 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ARGAN OIL (UNII: 4V59G5UW9X)
- JOJOBA OIL (UNII: 724GKU717M)
- SHEA BUTTER (UNII: K49155WL9Y)
- CUCUMBER (UNII: YY7C30VXJT)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
What is the NDC to RxNorm Crosswalk for Pearlessence Hand Wash Coconut And Rose?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
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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".