CIMETIDINE 10% / LIDOCAINE 5% / SALICYLIC ACID 40%- cimetidine 10% / lidocaine 5% / salicylic acid 40% cream 
Sincerus Florida, LLC

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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CIMETIDINE 10% / LIDOCAINE 5% / SALICYLIC ACID 40%

Directions for Use

c

Sincerus Florida, LLC adverse reactions.

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Active, inactive

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NDC 72934-2046-2 CIMETIDINE USP 10% / LIDOCAINE USP 5% / SALICYLIC ACID USP 40%
Cream 30 gm

f

CIMETIDINE 10% / LIDOCAINE 5% / SALICYLIC ACID 40% 
cimetidine 10% / lidocaine 5% / salicylic acid 40% cream
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-2046
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 g  in 100 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 g  in 100 g
CIMETIDINE (UNII: 80061L1WGD) (CIMETIDINE - UNII:80061L1WGD) CIMETIDINE10 g  in 100 g
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-2046-230 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-2046)

Revised: 4/2019
Document Id: 874cd0d1-8712-225c-e053-2995a90af24b
Set id: 874cd0d1-8711-225c-e053-2995a90af24b
Version: 1
Effective Time: 20190424
 
Sincerus Florida, LLC