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
- PEPPERMINT; TEA TREE OIL; WITCH HAZEL
- Active strength
- .1; .04; .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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- XIMONTH Quick Essence
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PEPPERMINT | .1 mg/20mg |
| TEA TREE OIL | .04 mg/20mg |
| WITCH HAZEL | .6 mg/20mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V95R5KMY2B, VIF565UC2G, 101I4J0U34 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84989-012-01 | XIMONTH Quick Essence | 20 mg in 1 BOTTLE, GLASS | LIQUID | 20 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| 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 | Historical |