Severe Congestion and Cough, Cold and Flu
Equate 44-004063-Delisted
Approved
Approval ID
a53ca6e5-f2cd-46fe-8b7c-87bfef48ac19
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 29, 2025
Manufacturers
FDA
WALMART INC.
DUNS: 051957769
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, Triprolidine HCl
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code79903-146
Application NumberM012
Product Classification
M
Marketing Category
C200263
G
Generic Name
Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, Triprolidine HCl
Product Specifications
Effective DateApril 29, 2025
FDA Product Classification