all day pain relief

Generic: naproxen sodium

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day pain relief
Generic Name naproxen sodium
Labeler h e b
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-068
Product ID 37808-068_cc1eb980-a014-48df-83cd-9cfa050b4414
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079096
Listing Expiration 2026-12-31
Marketing Start 2015-09-30

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 37808068
Hyphenated Format 37808-068

Supplemental Identifiers

RxCUI
849574
UPC
0041220284337
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 (source: ndc)
Application Number ANDA079096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

37808-068-24 1 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC 37808-068-50 1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc1eb980-a014-48df-83cd-9cfa050b4414", "openfda": {"upc": ["0041220284337"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["6dd54a14-67cd-4295-9bd5-1d6f8cb9316d"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-068-24)  / 24 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-068-24", "marketing_start_date": "20150930"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-068-50)  / 50 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-068-50", "marketing_start_date": "20150930"}], "brand_name": "All Day Pain Relief", "product_id": "37808-068_cc1eb980-a014-48df-83cd-9cfa050b4414", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-068", "generic_name": "Naproxen Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20150930", "listing_expiration_date": "20261231"}