maximum strength day cold and flu and night severe cold and flu

Generic: acetaminophe, dextromethorphan hbr, guaifenesin, phenylephrine hcl, triprolidine hcl tablets

Labeler: time cap laboratories,inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength day cold and flu and night severe cold and flu
Generic Name acetaminophe, dextromethorphan hbr, guaifenesin, phenylephrine hcl, triprolidine hcl tablets
Labeler time cap laboratories,inc
Dosage Form KIT
Manufacturer
TIME CAP LABORATORIES,INC

Identifiers & Regulatory

Product NDC 49483-726
Product ID 49483-726_fff69901-965d-5372-e053-6394a90a29c2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-09-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49483726
Hyphenated Format 49483-726

Supplemental Identifiers

RxCUI
1110988 2549037 2560237

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name maximum strength day cold and flu and night severe cold and flu (source: ndc)
Generic Name acetaminophe, dextromethorphan hbr, guaifenesin, phenylephrine hcl, triprolidine hcl tablets (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 1.25 mg
source: label
Packaging
  • 4 BLISTER PACK in 1 CARTON (49483-726-64) / 1 KIT in 1 BLISTER PACK * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

49483-726-64 4 BLISTER PACK in 1 CARTON (49483-726-64) / 1 KIT in 1 BLISTER PACK * 6 TABLET in 1 BLISTER PACK * 4 TABLET in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Maximum strength Day cold and flu and Night severe cold and flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "fff69901-965d-5372-e053-6394a90a29c2", "openfda": {"rxcui": ["1110988", "2549037", "2560237"], "spl_set_id": ["fff69901-965c-5372-e053-6394a90a29c2"], "manufacturer_name": ["TIME CAP LABORATORIES,INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (49483-726-64)  / 1 KIT in 1 BLISTER PACK *  6 TABLET in 1 BLISTER PACK *  4 TABLET in 1 BLISTER PACK", "package_ndc": "49483-726-64", "marketing_start_date": "20230921"}], "brand_name": "Maximum strength Day cold and flu and Night severe cold and flu", "product_id": "49483-726_fff69901-965d-5372-e053-6394a90a29c2", "dosage_form": "KIT", "product_ndc": "49483-726", "generic_name": "Acetaminophe, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, Triprolidine HCl Tablets", "labeler_name": "TIME CAP LABORATORIES,INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum strength Day cold and flu and Night severe cold and flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230921", "listing_expiration_date": "20261231"}