all day pain relief

Generic: naproxen sodium tablets, 220 mg

Labeler: healthlife of usa llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium tablets, 220 mg
Labeler healthlife of usa llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
HealthLife of USA LLC

Identifiers & Regulatory

Product NDC 69517-109
Product ID 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091353
Listing Expiration 2026-12-31
Marketing Start 2011-09-30

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 69517109
Hyphenated Format 69517-109

Supplemental Identifiers

RxCUI
849574
UPC
0069517109248
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 all day pain relief (source: ndc)
Generic Name naproxen sodium tablets, 220 mg (source: ndc)
Application Number ANDA091353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH
  • 400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTON
  • 25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH
  • 50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH
source: ndc

Packages (4)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "046b91ed-d78b-42c0-b822-77fcbdeff84b", "openfda": {"upc": ["0069517109248"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["7b0cb91e-5465-40ef-9f82-919f7d984f17"], "manufacturer_name": ["HealthLife of USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 POUCH (69517-109-02)  / 2 TABLET in 1 POUCH", "package_ndc": "69517-109-02", "marketing_start_date": "20160407"}, {"sample": false, "description": "400 BOTTLE in 1 BOTTLE (69517-109-04)  / 100 BOTTLE in 1 BOTTLE (69517-109-01)  / 24 CARTON in 1 BOTTLE (69517-109-24)  / 1 TABLET in 1 CARTON", "package_ndc": "69517-109-04", "marketing_start_date": "20160407"}, {"sample": false, "description": "25 POUCH in 1 BOX (69517-109-25)  / 2 TABLET in 1 POUCH", "package_ndc": "69517-109-25", "marketing_start_date": "20160407"}, {"sample": false, "description": "50 POUCH in 1 BOX (69517-109-50)  / 2 TABLET in 1 POUCH", "package_ndc": "69517-109-50", "marketing_start_date": "20160407"}], "brand_name": "All Day Pain Relief", "product_id": "69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69517-109", "generic_name": "Naproxen Sodium Tablets, 220 mg", "labeler_name": "HealthLife of USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20110930", "listing_expiration_date": "20261231"}