FDA.reportPublic FDA data

Sovereign Silver Foaming Facial Cleanser

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 Foaming Facial Cleanser
Active ingredientSALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1%

OTC - PURPOSE SECTION

Acne treatment

INDICATIONS & USAGE SECTION

USES for treatment of acne.Penetrates pores to eliminate most acne blemishes,blackheads and whiteheads.

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

When using this product. skin irritation and dryness is more likely to occcur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medicarion a 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 reach of children. If swallowed, get medical help or contact Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions Take a quarter sized amount of the product in wet hands and work into a fine lather.Apply to wet face and massage for 60 seconds. Rinse with warm water and pat the skin dry. Use twice daily.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Capryloyl/Caproyl Methyl Glucamide, Citric Acid, Coco-Glucoside, Cocos Nucifera(Coconut)Fruit Extract, Glycerin, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Jojoba Esters, Lactobacillus,Lactobacillus Ferment, Lauroyl/Myristoyl Methyl Glucamide, Propanediol, Salix Alba(Willow) Bark Extract, Silver, Sodium Citrate, Sunfloweroyl Methylglucamide, Water, Xanthan Gum.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foaming Facial Cleanser Exfoliating washFoaming Facial Cleanser Exfoliating wash

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52166-01652166-016-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
LIMOSILACTOBACILLUS FERMENTUM2C1F12C6APIACT
XANTHAN GUMTTV12P4NEEIACT
PROPANEDIOL5965N8W85TIACT
SILVER3M4G523W1GIACT
COCONUT JUICEAMN6S4M09GIACT
LAUROYL/MYRISTOYL METHYL GLUCAMIDESC667B999PIACT
CAPRYLOYL/CAPROYL METHYL GLUCAMIDE0451R360HRIACT
COCO GLUCOSIDEICS790225BIACT
SALIX ALBA BARK205MXS71H7IACT
SODIUM CITRATE1Q73Q2JULRIACT
SUNFLOWER OIL3W1JG795YIIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SALICYLIC ACIDO414PZ4LPZACTIB
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70)96YYQ5TK1KIACT
HAMAMELIS VIRGINIANA TOPUDA30A2JJYIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1d770a10-a9e9-94c4-e063-6294a90a137a010579a1-cf6c-e041-e063-6294a90aaca92024-07-17WarningsExact identifier
spl set id: 010579a1-cf6c-e041-e063-6294a90aaca9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.