SOVEREIGN SILVER ACNE SPOT TREATMENT MEDICATED SERUM- salicylic acid liquid

Sovereign Silver Acne Spot Treatment Medicated Serum by

Drug Labeling and Warnings

Sovereign Silver Acne Spot Treatment Medicated Serum by is a Otc medication manufactured, distributed, or labeled by Natural Immunogenics Corporation, Inspec Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2%

PURPOSE

Acne treatment

INDICATIONS & USAGE

Uses for treatment of acne. Clears acne blemishes ans allows skin to heal. Helps prevent acne blemishes.

WARNINGS

For external use only.

WHEN USING

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.

STOP USE

Stop use and ask a doctor if. skin irritation occurs or gets worse.

KEEP OUT OF REACH OF CHILDREN

Keep out of children. If swallowed, get medical help or contact Poison Control Center right away.

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOVEREIGN SILVER ACNE SPOT TREATMENT MEDICATED SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52166-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 29 mL

Inactive Ingredients
Ingredient Name	Strength
PROPANEDIOL (UNII: 5965N8W85T)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
ZINC (UNII: J41CSQ7QDS)
COCONUT JUICE (UNII: AMN6S4M09G)
SILVER (UNII: 3M4G523W1G)
XANTHAN GUM (UNII: TTV12P4NEE)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ARGININE (UNII: 94ZLA3W45F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52166-017-01	29 mL in 1 TUBE; Type 0: Not a Combination Product	07/24/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	07/24/2023

Labeler - Natural Immunogenics Corporation (048744085)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(52166-017)