NDC 50254-365

Bea-Silky

Alcohol

Bea-Silky is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Beaver Research Company. The primary component is Alcohol.

Product ID50254-365_bff3b23b-ffe9-4644-a266-65e4ac412389
NDC50254-365
Product TypeHuman Otc Drug
Proprietary NameBea-Silky
Generic NameAlcohol
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2015-01-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333E
Labeler NameBeaver Research Company
Substance NameALCOHOL
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50254-365-09

2000 mL in 1 CARTRIDGE (50254-365-09)
Marketing Start Date2015-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50254-365-27 [50254036527]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-12 [50254036512]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-09 [50254036509]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-24 [50254036524]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-28 [50254036528]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-01 [50254036501]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-08 [50254036508]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-15 [50254036515]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-10 [50254036510]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-05 [50254036505]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-11 [50254036511]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-06 [50254036506]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-17 [50254036517]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-55 [50254036555]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-03 [50254036503]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-14 [50254036514]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-07 [50254036507]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

NDC 50254-365-13 [50254036513]

Bea-Silky LOTION
Marketing CategoryOTC monograph not final
Application Numberpart333E
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALCOHOL.7 mL/mL

OpenFDA Data

SPL SET ID:3c597de8-df5d-499a-8f40-bd301bff30a0
Manufacturer
UNII

NDC Crossover Matching brand name "Bea-Silky" or generic name "Alcohol"

NDCBrand NameGeneric Name
50254-365Bea-SilkyBea-Silky
0363-0370Advanced Hand SanitizerAlcohol
0363-9776Advanced Hand SanitizerAlcohol
0363-0046AlcoholAlcohol
0074-9857Alcohol - Hand SanitizerAlcohol
0065-8000Alcohol Antiseptic 80%Alcohol
0404-0122Antibacterialalcohol
0395-0040Ethyl Rubbing AlcoholAlcohol
0363-0968Hand SanitizerALCOHOL
0219-2020Humphreys Alcoholado MaravillaALCOHOL
0404-5988Instant Hand Sanitizeralcohol
0295-9025Nozin Nasal SanitizerAlcohol
0362-6000SeptoSanAlcohol
0362-6001SeptoSanAlcohol
0362-6002SeptoSanAlcohol
0064-1050TRISEPTINALCOHOL
0363-1305WalgreensAlcohol
0363-1306WalgreensAlcohol
0363-1307WalgreensAlcohol
0363-1308WalgreensAlcohol
0363-1309WalgreensAlcohol
0363-0969Walgreens Advanced Hand Sanitizer Citrus ScentAlcohol
0363-9005Walgreens Advanced Hand Sanitizer Made with Plant-Based Ethyl AlcoholAlcohol
0363-9003Walgreens Advanced Hand Sanitizer with Aloe and Vitamin EAlcohol
0363-0967WALGREENS ADVANCED HAND SANITIZER WITH FRESH SCENTALCOHOL
0363-9004Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
0363-9008Walgreens Advanced Hand Sanitizer with Vitamin EAlcohol
0363-9006Walgreens Hand Sanitizer Coastal Breeze ScentAlcohol
0363-9007Walgreens Hand Sanitizer Crisp Apple ScentAlcohol
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