LET ME CLARIFY- salicylic acid gel 
mybody

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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ACTIVE INGREDIENTS

SALICYLIC ACID 2%

PURPOSE

ACNE TREATMENT

USE FOR THE TREATMENT OF ACNE

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE * IF YOU HAVE VERY SENSITIVE SKIN OR ARE SENSITIVE TO SALICYLIC ACID.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF

WHEN USING THIS PRODUCT

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

OTHER INFORMATION

* AVOID STORAGE AT EXTREME TEMPERATURES (BELOW 40°F AND ABOVE 100°F).

INACTIVE INGREDIENTS: WATER, BUTYLENE GLYCOL, GLYCOLIC ACID, POLYQUATERNIUM 10, EUCALYPTUS GLOBULUS OIL, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, ACETYL CARBOXYMETHYL COCOYL GLYCINE, MYRISTOYL TETRAPEPTIDE-13, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, PENTYLENE GLYCOL, POTASSIUM HYDROXIDE.

QUESTIONS OR COMMENTS?

CALL 877.423.1314 * WWW.LOVEMYBODY.COM

5-8 x 2_5ml Die-Line_LET ME CLARIFY_V3_10.24.11Let-Me-Clarify_Drug-Facts-Box

LET ME CLARIFY 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49520-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
1,3-BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
ACETYL CARBOXYMETHYL COCOYL GLYCINE (UNII: 3TNX4P92J3)  
MYRISTOYL TETRAPEPTIDE-4 (UNII: 87AV1IB2EU)  
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49520-103-1130 mL in 1 BOTTLE
2NDC:49520-103-315 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D09/24/2012
Labeler - mybody (004460532)

Revised: 12/2013
Document Id: f646e74c-7e69-4992-b8d2-0e9661930c82
Set id: 8e36c36f-aa9e-4ae2-8dea-53d167e81a7f
Version: 6
Effective Time: 20131230
 
mybody