maximum strength non drowsy day and night cold and flu

Generic: maximum strength non drowsy day and night cold and flu

Labeler: wal-mart stores inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength non drowsy day and night cold and flu
Generic Name maximum strength non drowsy day and night cold and flu
Labeler wal-mart stores inc
Dosage Form KIT
Manufacturer
WAL-MART STORES INC

Identifiers & Regulatory

Product NDC 49035-674
Product ID 49035-674_4948f8ec-a55e-c624-e063-6394a90a49f8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2020-11-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49035674
Hyphenated Format 49035-674

Supplemental Identifiers

RxCUI
1086997 1297288 2634363

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 non drowsy day and night cold and flu (source: ndc)
Generic Name maximum strength non drowsy day and night cold and flu (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (49035-674-16) * 1 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-245-12) * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-246-04)
source: ndc

Packages (1)

49035-674-16 1 KIT in 1 CARTON (49035-674-16) * 1 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-245-12) * 1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-246-04)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Maximum Strength Non Drowsy Day and Night Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "4948f8ec-a55e-c624-e063-6394a90a49f8", "openfda": {"rxcui": ["1086997", "1297288", "2634363"], "spl_set_id": ["d6a35fb8-1899-4da2-ad2b-0423e332845d"], "manufacturer_name": ["WAL-MART STORES INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (49035-674-16)  *  1 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-245-12)  *  1 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (79903-246-04)", "package_ndc": "49035-674-16", "marketing_start_date": "20201116"}], "brand_name": "Maximum Strength Non Drowsy Day and Night Cold and Flu", "product_id": "49035-674_4948f8ec-a55e-c624-e063-6394a90a49f8", "dosage_form": "KIT", "product_ndc": "49035-674", "generic_name": "Maximum Strength Non Drowsy Day and Night Cold and Flu", "labeler_name": "WAL-MART STORES INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Non Drowsy Day and Night Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201116", "listing_expiration_date": "20271231"}