RITE AID RENEWAL - salicylic acid cream 
RITE AID 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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DRUG FACTS

ACTIVE INGREDIENT

SALICYLIC ACID 2.0%

PURPOSE

ACNE TREATMENT

USES

For the treatment of Acne

WARNINGS

FOR EXTERNAL USE ONLY

ASK DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR  CONTACT POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

CLEANSE TWO TIMES A DAY. WET FACE. APPLY TO HANDS ADD WATER AND WORK INTO LATHER. MASSAGE FACE GENTLY. RINSE WELL.

QUESTIONS OR COMMENTS

1-866-695-3030

INACTIVE INGREDIENTS

WATER, CETYL ALCOHOL, PPG-15 STEARYL ETHER, POLYETHYLENE, GLYCOLIC ACID, GLYCERIN, POLYSORBATE 60, STEREATH-21, C12-15 ALKYL LACTATE, CETYL LACTATE, BHT, NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE, COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, POTASSIUM CETYL PHOSPHATE, DISODIUM EDTA, XANTHAN GUM, SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE, SODIUM HYDROXIDE, AGAR, MENTHOL, BENZALKONIUM CHLORIDE, MICA, TITANIUM DIOXIDE, RED 40 (CI 16035), RED 33  (CI 17200), YELLOW 5 (CI 19140),  FRAGRANCE  (PARFUM)

LABEL COPY

image of the label

RITE AID RENEWAL 
salicylic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-8210
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARETH-15 (UNII: O6V041E38J)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
STEARETH-21 (UNII: 53J3F32P58)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
AGAR (UNII: 89T13OHQ2B)  
MENTHOL (UNII: L7T10EIP3A)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-8210-5125 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/03/2011
Labeler - RITE AID CORPORATION (014578892)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 7/2011
Document Id: 6860f233-ca92-4867-a484-3b854ba92a45
Set id: 6e53dad7-5fa8-4fe1-ac6d-11921458d6a0
Version: 1
Effective Time: 20110729
 
RITE AID CORPORATION