up and up arthritis pain reliever

Generic: diclofenac sodium

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

Drug Facts

Product Profile

Brand Name up and up arthritis pain reliever
Generic Name diclofenac sodium
Labeler target corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diclofenac sodium 10 mg/g

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-569
Product ID 11673-569_3f9d13e9-6d6c-41cd-b2ba-9567247172eb
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211253
Listing Expiration 2026-12-31
Marketing Start 2020-08-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673569
Hyphenated Format 11673-569

Supplemental Identifiers

RxCUI
855633
UNII
QTG126297Q

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 up and up arthritis pain reliever (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA211253 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (11673-569-01) / 100 g in 1 TUBE
  • 1 TUBE in 1 CARTON (11673-569-03) / 150 g in 1 TUBE
source: ndc

Packages (2)

11673-569-01 1 TUBE in 1 CARTON (11673-569-01) / 100 g in 1 TUBE 11673-569-03 1 TUBE in 1 CARTON (11673-569-03) / 150 g in 1 TUBE

Ingredients (1)

diclofenac sodium (10 mg/g)

Linked Drug Pages (1)

up and up arthritis pain reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3f9d13e9-6d6c-41cd-b2ba-9567247172eb", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["0b7ae58c-cdaf-4343-a199-7a90bf901eb5"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (11673-569-01)  / 100 g in 1 TUBE", "package_ndc": "11673-569-01", "marketing_start_date": "20200819"}, {"sample": false, "description": "1 TUBE in 1 CARTON (11673-569-03)  / 150 g in 1 TUBE", "package_ndc": "11673-569-03", "marketing_start_date": "20210318"}], "brand_name": "up and up arthritis pain reliever", "product_id": "11673-569_3f9d13e9-6d6c-41cd-b2ba-9567247172eb", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-569", "generic_name": "diclofenac sodium", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up arthritis pain reliever", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA211253", "marketing_category": "ANDA", "marketing_start_date": "20200819", "listing_expiration_date": "20261231"}