NDC 0363-0542

Mucus Relief PE

Guaifenesin, Phenylephrine Hcl

Mucus Relief PE is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Guaifenesin; Phenylephrine Hydrochloride.

Product ID0363-0542_386ccc61-0815-459d-8822-6637a45b187d
NDC0363-0542
Product TypeHuman Otc Drug
Proprietary NameMucus Relief PE
Generic NameGuaifenesin, Phenylephrine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2006-04-15
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameWalgreen Company
Substance NameGUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient Strength400 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0363-0542-01

1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Start Date2006-04-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0542-25 [00363054225]

Mucus Relief PE TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2006-04-15

NDC 0363-0542-01 [00363054201]

Mucus Relief PE TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2006-04-15

NDC 0363-0542-11 [00363054211]

Mucus Relief PE TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2006-04-15
Marketing End Date2016-03-28

NDC 0363-0542-10 [00363054210]

Mucus Relief PE TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2006-04-15
Marketing End Date2016-03-28

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN400 mg/1

OpenFDA Data

SPL SET ID:cb1c1922-5dc6-520d-e77e-e951726d9701
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1304111

    • NDC Crossover Matching brand name "Mucus Relief PE" or generic name "Guaifenesin, Phenylephrine Hcl"

    NDCBrand NameGeneric Name
    0363-0542Mucus Relief PEGuaifenesin, Phenylephrine HCl
    21130-542Mucus Relief PEGuaifenesin and Phenylephrine HCl
    68016-686Mucus Relief PEGuaifenesin, Phenylephrine HCl
    76864-209BACZOL EXPECTORANTGUAIFENESIN, PHENYLEPHRINE HCl
    45737-606BiophexGuaifenesin, Phenylephrine HCl
    58552-336GilphexGuaifenesin, Phenylephrine HCl
    66576-336GilphexGuaifenesin, Phenylephrine HCl
    58552-332Giltuss Sinus and Chest CongestionGuaifenesin, Phenylephrine HCl
    70000-0141Mucus Relief PE Sinus CongestionGuaifenesin, Phenylephrine HCl
    59779-548Non-Drying Sinus PEGuaifenesin, Phenylephrine HCl
    21130-927Sinus PEGuaifenesin, Phenylephrine HCl
    50844-548Sinus Relief PEGuaifenesin, Phenylephrine HCl
    54859-605Tusnel Pediatric DropsGuaifenesin, Phenylephrine HCl
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