OTC - ACTIVE INGREDIENT SECTION
Salicylic Acid 2%
Sovereign Silver Acne Spot Treatment Medicated Serum
- Manufacturer
- Natural Immunogenics Corporation | Inspec Solutions
- Effective date
- 2023-09-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:25:51
Label at a glance#
ProductSovereign Silver Acne Spot Treatment Medicated Serum
Active ingredientSALICYLIC ACID
Label structure10 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Acne treatment
INDICATIONS & USAGE SECTION
Uses for treatment of acne. Clears acne blemishes ans allows skin to heal. Helps prevent acne blemishes.
WARNINGS SECTION
For external use only.
OTC - WHEN USING SECTION
When usin this product. Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medicarion at a time.
OTC - STOP USE SECTION
Stop use and ask a doctor if. skin irritation occurs or gets worse.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of children. If swallowed, get medical help or contact Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions After cleansing, cover the affected area with a thin layer of product. Start with one application a day and then gradually increase to two or three applications daily if needed,or as directed by a doctor.
INACTIVE INGREDIENT SECTION
Inactive Ingredients Arginine, Cocos Nucifera(Coconut) Fruit Extract,Glycerin,Hydrolized Sodium Hyaluronate,Lactobacillus, Lactobacillus Ferment, Niacinamide,Panthenol, Propanediol, Sodium Citrate, Silver, Water, Xanthan Gum, Zinc PCA
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Sovereign Silver Acne Spot Treatment Medicated Serum
- Salicylic Acid
- PROPANEDIOL
- PANTHENOL
- GLYCERIN
- LIMOSILACTOBACILLUS FERMENTUM
- SODIUM CITRATE
- ZINC
- COCONUT JUICE
- SILVER
- XANTHAN GUM
- HYALURONATE SODIUM
- ARGININE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 52166-017 | 52166-017-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PROPANEDIOL | 5965N8W85T | IACT |
| PANTHENOL | WV9CM0O67Z | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| LIMOSILACTOBACILLUS FERMENTUM | 2C1F12C6AP | IACT |
| SALICYLIC ACID | O414PZ4LPZ | ACTIB |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| ZINC | J41CSQ7QDS | IACT |
| COCONUT JUICE | AMN6S4M09G | IACT |
| SILVER | 3M4G523W1G | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| HYALURONATE SODIUM | YSE9PPT4TH | IACT |
| ARGININE | 94ZLA3W45F | 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 |
|---|---|---|---|---|---|---|
| 1d76ee97-7804-9289-e063-6294a90a7787 | 013d93cd-7342-a5db-e063-6294a90a5123 | 2024-07-17 | Warnings | 013d93cd-7342-a5db-e063-6294a90a5123 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.