NDC 49580-0192

Day Time Cold Multi-Symptom Cool Blast

Tylenol Multi Symptom Cool Blast Daytime

Day Time Cold Multi-Symptom Cool Blast is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by P & L Development, Llc. The primary component is Acetaminophen; Guaifenesin; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.

Product ID49580-0192_74a22e35-bdfe-4705-bf6d-7195d4ef6275
NDC49580-0192
Product TypeHuman Otc Drug
Proprietary NameDay Time Cold Multi-Symptom Cool Blast
Generic NameTylenol Multi Symptom Cool Blast Daytime
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-01-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameP & L Development, LLC
Substance NameACETAMINOPHEN; GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength325 mg/5mL; mg/5mL; mg/5mL; mg/5mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 49580-0192-8

237 mL in 1 BOTTLE, PLASTIC (49580-0192-8)
Marketing Start Date2010-01-01
Marketing End Date2021-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49580-0192-8 [49580019208]

Day Time Cold Multi-Symptom Cool Blast LIQUID
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-01
Marketing End Date2021-12-30

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN325 mg/5mL

OpenFDA Data

SPL SET ID:7d7cbf19-6533-4788-8dc8-e8bb9d116447
Manufacturer
UNII
UPC Code
  • 0715256801928

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