NDC 52191-351

Urea

Urea

Urea is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Bowyn Labs, Llc. The primary component is Urea.

Product ID52191-351_69ac5657-d5b3-1abc-e053-2991aa0a26d7
NDC52191-351
Product TypeHuman Prescription Drug
Proprietary NameUrea
Generic NameUrea
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2018-04-12
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameBowyn Labs, LLC
Substance NameUREA
Active Ingredient Strength410 mg/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 52191-351-08

227 g in 1 BOTTLE, PLASTIC (52191-351-08)
Marketing Start Date2018-04-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52191-351-08 [52191035108]

Urea CREAM
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2018-04-12

Drug Details

Active Ingredients

IngredientStrength
UREA410 mg/g

OpenFDA Data

SPL SET ID:69ac5657-d5b2-1abc-e053-2991aa0a26d7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1436933
    • UPC Code
  • 0352191351080

    • NDC Crossover Matching brand name "Urea" or generic name "Urea"

    NDCBrand NameGeneric Name
    15631-0449UREAUREA
    42192-101UREAUREA
    42291-849UREAUREA
    42792-101UREAUREA
    42808-202UREAUREA
    42808-204UreaUrea
    44523-617UREAurea
    50268-872UREAUREA
    51862-181UreaUrea
    52187-549UREAUREA
    52191-351UreaUREA
    54295-308UREAUREA
    68428-688UreaUrea
    71399-4528UREAUREA
    54295-312UREAUREA
    54295-311UREAUREA
    71919-694UREAUREA
    63629-2040UREAUREA
    63629-2039UREAUREA
    63629-2036UREAUREA
    63629-2037UREAUREA
    63629-2038UREAUREA
    42546-100CEM-Ureaurea
    10481-3005GORDONS UREA 40UREA
    50268-820Urea 20Urea
    50096-501Urea 47% CreamUREA
    0904-7167Urea Cream 40%Urea
    16477-340Urea Cream 40%Urea
    16477-341Urea Cream 41%Urea
    42192-115UREA HYDRATING TOPICALUREA
    42361-043YouGreen FUrea
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