Diclona Gel
- Product NDC
- 72189-688
- 11-digit product format
- 721890688
- Labeler code
- 72189
- Product ID
- 72189-688_5b126754-a96e-4810-e063-6294a90aee51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclona Gel
- Dosage form
- GEL
- Route
- CUTANEOUS
- Labeler
- Direct_Rx
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-09-09
- Substance
- DICLOFENAC SODIUM; LIDOCAINE
- Active strength
- .01; .045 g/g; g/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Anti-Inflammatory Agents, Non-Steroidal [CS], Antiarrhythmic [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Local Anesthesia [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Diclona Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICLOFENAC SODIUM | .01 g/g |
| LIDOCAINE | .045 g/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-688-35 | 72189068835 | 99 g in 1 TUBE (72189-688-35) | 99 g | 2026-09-09 | No | No | Current |