Wart Remover
- Product NDC
- 88073-221
- Requested package NDC
- 88073-221-12
- 11-digit product format
- 880730221
- Labeler code
- 88073
- Product ID
- 88073-221_5d76c06d-83bc-ac53-e063-6394a90aa858
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Wart Remover
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Labeler
- Shenzhen Fanshi Technology Co., Ltd.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-10-10
- Substance
- SALICYLIC ACID
- Active strength
- .17 g/1
- 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
- Wart Remover
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | .17 g/1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 88073-221-12 | 88073022112 | 5 BAG in 1 BOX (88073-221-12) / 1 LIQUID in 1 BAG | 5 bag | 2026-10-10 | No | No | Current |