XIMONTH Quick Essence
- Product NDC
- 84989-012
- 11-digit product format
- 849890012
- Labeler code
- 84989
- Product ID
- 84989-012_448b7147-f046-c50a-e063-6294a90a2f75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shantou Ximonth Biotechnology Co., Ltd.
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-30
- Substance
- TEA TREE OIL; PEPPERMINT; WITCH HAZEL
- Active strength
- .04; .1; .6 mg/20mg; mg/20mg; mg/20mg
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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
- XIMONTH Quick Essence
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| TEA TREE OIL | .04 mg/20mg |
| PEPPERMINT | .1 mg/20mg |
| WITCH HAZEL | .6 mg/20mg |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| VIF565UC2G | Internal UNII lookup |
| V95R5KMY2B | Internal UNII lookup |
| 101I4J0U34 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4256f607-c9cf-cd0f-e063-6394a90a5487 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| dea2eded-d1e7-46bb-9a3d-f8dc20de6277 | Product name | 1 | 20190408 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84989-012-01 | XIMONTH Quick Essence | 20 mg in 1 BOTTLE, GLASS | LIQUID | 20 | 2 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ulensy Corn Callus and Wart Remover | CORN CALLUS AND WART REMOVER | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 0f3353ef-e105-7bd4-e063-6394a90a2562 | 2024-01-18 | Warnings | M028 |
| WARTRIN Wart Remover | SALICYLIC ACID | BALBOA COMPANIES LLC | 62c99f48-3dc1-4b41-8bc4-e93e2decadd9 | 2023-11-11 | Warnings | M028 |
| UFORIC Wart Remover | SALICYLIC ACID | UFORIC HEALTH LLC | 0d06cac6-5296-4d8a-b59e-966baac6be5f | 2023-11-06 | Warnings | M028 |
| WARTOVIR Wart Remover | SALICYLIC ACID | BALBOA COMPANIES LLC | 2dbf5b40-d759-4c37-8dfe-3b65a7e6dbb6 | 2023-11-06 | Warnings | M028 |
| VerruStat Wart Remover | SALICYLIC ACID | Clinical Therapeutic Solutions | 16607d6e-6a5f-4b03-b38c-3610aef9b165 | 2023-11-05 | Warnings | M028 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 84989-012-01 | 84989001201 | 20 mg in 1 BOTTLE, GLASS (84989-012-01) | 20 mg | 2025-10-30 | No | No | Current |