SOVEREIGN SILVER FOAMING FACIAL CLEANSER- salicylic acid/acne treatment gel gel 
Natural Immunogenics Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SOVEREIGN SILVER Foaming Facial Cleanser Exfoliating Wash 1% Salicylic Acid/Acne treatment Gel

Salicylic Acid 1%

Acne treatment

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

Warnings

For external use only.

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.

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

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

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 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.

Foaming Facial Cleanser Exfoliating wash

SOVEREIGN SILVER FOAMING FACIAL CLEANSER 
salicylic acid/acne treatment gel gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52166-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 59 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PROPANEDIOL (UNII: 5965N8W85T)  
SILVER (UNII: 3M4G523W1G)  
COCONUT JUICE (UNII: AMN6S4M09G)  
LAUROYL/MYRISTOYL METHYL GLUCAMIDE (UNII: SC667B999P)  
CAPRYLOYL/CAPROYL METHYL GLUCAMIDE (UNII: 0451R360HR)  
COCO GLUCOSIDE (UNII: ICS790225B)  
SALIX ALBA BARK (UNII: 205MXS71H7)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70) (UNII: 96YYQ5TK1K)  
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52166-016-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product07/24/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D07/24/2023
Labeler - Natural Immunogenics Corporation (048744085)
Establishment
NameAddressID/FEIBusiness Operations
Inspec Solutions081030372manufacture(52166-016)

Revised: 9/2023
Document Id: 05e1cf85-6b19-57fe-e063-6294a90a55fc
Set id: 010579a1-cf6c-e041-e063-6294a90aaca9
Version: 2
Effective Time: 20230921
 
Natural Immunogenics Corporation