first aid direct all day pain relief

Generic: naproxen sodium

Labeler: cintas corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name first aid direct all day pain relief
Generic Name naproxen sodium
Labeler cintas corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Cintas Corporation

Identifiers & Regulatory

Product NDC 42961-122
Product ID 42961-122_dc86ba45-5462-4c1b-9a65-4bcf25e0e43b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Listing Expiration 2026-12-31
Marketing Start 2023-07-19

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42961122
Hyphenated Format 42961-122

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

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 first aid direct all day pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)
source: ndc

Packages (1)

42961-122-02 25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

First Aid Direct All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc86ba45-5462-4c1b-9a65-4bcf25e0e43b", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["1c9384c1-52f8-4482-88fc-5f5b6d770c42"], "manufacturer_name": ["Cintas Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 PACKET in 1 BOX (42961-122-02)  / 1 TABLET, COATED in 1 PACKET (42961-122-01)", "package_ndc": "42961-122-02", "marketing_start_date": "20230719"}], "brand_name": "First Aid Direct All Day Pain Relief", "product_id": "42961-122_dc86ba45-5462-4c1b-9a65-4bcf25e0e43b", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "42961-122", "generic_name": "Naproxen Sodium", "labeler_name": "Cintas Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "First Aid Direct All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}