CLEAR 40 PLUS SA- urea gel 
SSG Ventures Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Clear 40 Plus SA

Label

ACTIVE INGREDIENTS:

UREA 40%, SALICYLIC ACID 2%, TEA TREE OIL, ALOE VERA

SOOTHES ROUGH & DRY SKIN

HEALS CORNS & CALLOUSES

SOOTHES ROUGH & DRY SKIN

FOR EXTERNAL USE ONLY. AVOID CONTACT TO EYES.

KEEP OUT OF REACH OF CHILDREN. STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS.

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

KEEP OUT OF REACH OF CHILDREN.

APPLY TO AFFECTED AREA AT LEAST TWICE DAILY OR AS NEEDED.USE CONTINUOUSLY FOR 2-3 WEEKS FOR OPTIMAL RESULTS.

CARBOMER, XANTHAN GUM, MINERAL OIL, PROPYLENE GLYCOL,EMULSIFIERS, TRIETHANOLAMINE

KEEP LID FIRMLY CLOSED. STORE IN COOL DRY PLACE.

ENHANCED WITH TEA TREE OIL & ALOE VERA

APPLY TO AFFECTED AREA AT LEAST TWICE DAILY OR AS NEEDED.USE CONTINUOUSLY FOR 2-3 WEEKS FOR OPTIMAL RESULTS.

FOR EXTERNAL USE ONLY. AVOID CONTACT TO EYES. STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS.

CLEAR 40 PLUS SA 
urea gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81376-232
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
UREA (UNII: 8W8T17847W) (UREA - UNII:8W8T17847W) UREA40 g  in 113 g
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID6.5 g  in 113 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MINERAL OIL (UNII: T5L8T28FGP)  
COCONUT OIL (UNII: Q9L0O73W7L)  
WATER (UNII: 059QF0KO0R)  
TRIDECETH-10 (UNII: G624N6MSBA)  
TEA TREE OIL (UNII: VIF565UC2G)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Colorwhite (Opaque White) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81376-232-01113 g in 1 JAR; Type 0: Not a Combination Product09/20/2019
2NDC:81376-232-02226 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/20/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/20/2019
Labeler - SSG Ventures Inc (047626115)
Establishment
NameAddressID/FEIBusiness Operations
SSG Ventures Inc047626115manufacture(81376-232)

Revised: 4/2021
Document Id: c0f773bd-c60d-8864-e053-2a95a90a4524
Set id: bb63c54c-2c59-38f7-e053-2995a90a940c
Version: 2
Effective Time: 20210427
 
SSG Ventures Inc