Storage and handling
Store in a cool and dry place.
SOUTH MOON Numbing Cream
- Manufacturer
- Shantou South Moon Biotechnology Co., Ltd.
- Effective date
- 2026-03-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:50:47
Label at a glance#
ProductSOUTH MOON Numbing Cream
Active ingredientEUCALYPTUS GLOBULUS LEAF, ARNICA MONTANA FLOWER, EMU OIL
Label structure10 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ARNICA MONTANA FLOWER、EUCALYPTUS GLOBULUS LEAF、EMU OIL
OTC - PURPOSE SECTION
1. Local care: Suitable for local application, bringing a soothing and light experience.
2. Daily use: Can be matched with the care process to adapt to different life rhythms.
3. Refreshing and non-greasy: The paste has good ductility and feels dry and soft after application.
4. Convenient operation: The hose design is convenient and more efficient for outdoor use.
5. Quick absorption after application, the skin condition is softer and smoother.
6. Flexible application method, suitable for key adjustment of different parts.
7. The paste is highly stable and convenient for daily storage and use.
8. It can be used in the care steps after cleaning the skin.
9. Suitable for zoning care arrangements in the skin care process.
10. Suitable for a variety of skin types, feel comfortable and balanced skin.
11. No cumbersome tools are required, and the target area can be applied directly.
12. The rhythm of use is controllable, suitable for daily rhythms in multiple scenes.
13. The texture is delicate, and a light layer can cover the target area.
14. The paste is stable and not easy to deteriorate, so it is convenient to keep it for a long time.
15. Use it with other daily products for a more complete and comfortable experience.
OTC - WHEN USING SECTION
Provides tattoo pain relief; Relieves itching and pain; Relieves skin discomfort; Suitable for sensitive skin; Supports better skin recovery
WARNINGS SECTION
Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.
OTC - DO NOT USE SECTION
Discontinue use if signs of irritation or rash occur.
OTC - STOP USE SECTION
Discontinue use if signs of irritation or rash occur.
STORAGE AND HANDLING SECTION
Store in a cool and dry place.
INACTIVE INGREDIENT SECTION
WATER、GLYCERIN、MINERAL OIL、GLYCERYL MONOSTEARATE、1,2-HEXANEDIOL、CARBOMER HOMOPOLYMER TYPE A、TROLAMINE、ALLANTOIN
DOSAGE & ADMINISTRATION SECTION
Provides tattoo pain relief; Relieves itching and pain; Relieves skin discomfort; Suitable for sensitive skin; Supports better skin recovery
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | SO-B07-0375-01 | SO-B07-0375-01.jpg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84983-024-01 | SOUTH MOON Numbing Cream | 50 mg in 1 BOTTLE, PLASTIC | CREAM | 50 | 1 |
Products#
Every source-derived product name is available through these pages.
- SOUTH MOON Numbing Cream
- GLYCERIN
- EUCALYPTUS GLOBULUS LEAF
- ARNICA MONTANA FLOWER
- EMU OIL
- WATER
- 1,2-HEXANEDIOL
- TROLAMINE
- ALLANTOIN
- CARBOMER HOMOPOLYMER TYPE A
- MINERAL OIL
- GLYCERYL MONOSTEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84983-024 | 84983-024-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EUCALYPTUS GLOBULUS LEAF | S546YLW6E6 | ACTIB |
| ARNICA MONTANA FLOWER | OZ0E5Y15PZ | ACTIB |
| EMU OIL | 344821WD61 | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| WATER | 059QF0KO0R | IACT |
| 1,2-HEXANEDIOL | TR046Y3K1G | IACT |
| TROLAMINE | 9O3K93S3TK | IACT |
| ALLANTOIN | 344S277G0Z | IACT |
| CARBOMER HOMOPOLYMER TYPE A | F68VH75CJC | IACT |
| MINERAL OIL | T5L8T28FGP | IACT |
| GLYCERYL MONOSTEARATE | 230OU9XXE4 | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 4d5d693a-fe3c-c20b-e063-6294a90addf8 | 4d5d693a-fe3b-c20b-e063-6294a90addf8 | 2026-03-19 | Warnings | 4d5d693a-fe3c-c20b-e063-6294a90addf8 4d5d693a-fe3b-c20b-e063-6294a90addf8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.