All Day Pain Relief

Orange BookUNIISPLATC G02CC02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHealthLife of USA LLC

CountryUS (United States)

ATC codeG02CC02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
6951710902
2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCH
ndc11
6951710904
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
ndc11
6951710925
25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCH
ndc11
6951710950
50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCH

Annotations

UNII (FDA Substance ID)

9TN87S3A3C

NAPROXEN SODIUM

RxCUI 142442

Orange Book

A091353

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9TN87S3A3C",
    "rxcui": "142442",
    "inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
    "display_name": "NAPROXEN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8889af37-8345-4358-994d-7d8b847f4874": {
      "match": "brand_token",
      "title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
      "spl_version": "6",
      "published_date": "2026-05-13"
    }
  },
  "productid": "69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84b",
  "productndc": "69517-109",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "091353",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "220MG",
        "product_no": "001",
        "approval_date": "Sep 20, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "All Day Pain Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA091353",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium Tablets, 220 mg",
  "start_marketing_date": "20110930",
  "active_numerator_strength": "220"
}

Related drugs

Other records sharing ATC code G02CC02.

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