SOUTH MOON Wart Remover
- Product NDC
- 84983-013
- 11-digit product format
- 849830013
- Labeler code
- 84983
- Product ID
- 84983-013_449f0055-426b-e0ea-e063-6294a90af1a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GLYCERIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shantou South Moon Biotechnology Co., Ltd.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-17
- Substance
- ALOE BARBADENSIS LEAF; CENTELLA ASIATICA TRITERPENOIDS; HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER
- Active strength
- .002; .01; .002 mg/10mg; mg/10mg; mg/10mg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SOUTH MOON Wart Remover
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALOE BARBADENSIS LEAF | .002 mg/10mg |
| CENTELLA ASIATICA TRITERPENOIDS | .01 mg/10mg |
| HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER | .002 mg/10mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZY81Z83H0X, 4YS74Q4G4J, 8FP93ED6H2 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84983-013-01 | SOUTH MOON Wart Remover | 10 mg in 1 BOTTLE | LIQUID | 10 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84983-013-01 | 84983001301 | 10 mg in 1 BOTTLE (84983-013-01) | 10 mg | 2025-09-17 | No | No | Current |