Arthritis Pain Reliever
- Product NDC
- 69256-012
- 11-digit product format
- 692560012
- Labeler code
- 69256
- Product ID
- 69256-012_52ee818c-e80f-4a22-96d1-bbba1d578ab0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diclofenac sodium
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Harris Teeter, LLC
- Application
- ANDA208077
- Marketing category
- ANDA
- Marketing start
- 2021-01-29
- Marketing end
- 2026-05-29
- Substance
- DICLOFENAC SODIUM
- Active strength
- 10 mg/g
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69256-012-17 | Arthritis Pain Reliever | 1 in 1 CARTON | GEL | 1 | | 4 |
| 69256-012-17 | Arthritis Pain Reliever | 50 g in 1 TUBE | GEL | 50 | | 4 |
| 69256-012-35 | Arthritis Pain Reliever | 100 g in 1 TUBE | GEL | 100 | | 4 |
| 69256-012-35 | Arthritis Pain Reliever | 1 in 1 CARTON | GEL | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-012 | ARTHRITIS PAIN RELIEVER (DICLOFENAC SODIUM) GEL [HARRIS TEETER, LLC] | 4 | Current NDC, Legacy NDC, 4 package rows | 20250306_c6ef9bbd-7fbd-4683-b065-5eced58873c7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69256-012-17 | 69256001217 | 1 TUBE in 1 CARTON (69256-012-17) / 50 g in 1 TUBE | 1 tube | 2021-01-29 | 2026-05-29 | No | No | Current |
| 69256-012-35 | 69256001235 | 1 TUBE in 1 CARTON (69256-012-35) / 100 g in 1 TUBE | 1 tube | 2021-01-29 | 2026-05-29 | No | No | Current |