Label: CVS MAXIMUM STRENGTH BOIL RELIEF- benzocaine ointment
- NDC Code(s): 59779-444-28
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated March 31, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CVS MAXIMUM STRENGTH BOIL RELIEF
benzocaine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-444 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g in 100 g Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) EUCALYPTUS OIL (UNII: 2R04ONI662) LANOLIN (UNII: 7EV65EAW6H) MENTHOL (UNII: L7T10EIP3A) THYMOL (UNII: 3J50XA376E) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-444-28 1 in 1 TUBE 10/13/2014 1 28 g in 1 BOX; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/13/2014 Labeler - CVS Pharmacy, Inc. (062312574)