Label: BENZOCAINE AND RESORCINOL cream
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-810-24 - Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
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 February 16, 2011
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only.
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When using this product avoid contact with the eyes
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Stop use and ask a doctor if condition worsens, or if symptoms persist
for more than 7 days or clear up and occur again within a few days
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Do not apply over large areas of the body
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- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients aloe barbadensis leaf extract, carbomer, cetyl
alcohol, cholecalciferol, fragrance, glyceryl stearate, isopropyl myristate, isopropyl
palmitate, isopropyl stearate, lanolin alcohol, methylparaben, mineral oil, PEG-100
stearate, propylene glycol, purified water, retinyl palmitate, sodium sulfite, tocopheryl
acetate, trisodium HEDTA, triethanolamine, zea mays (corn) oil
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BENZOCAINE AND RESORCINOL
benzocaine and resorcinol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-810 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 200 mg in 1 g RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL 20 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ISOPROPYL STEARATE (UNII: 43253ZW1MZ) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MINERAL OIL (UNII: T5L8T28FGP) POLYOXYL 100 STEARATE (UNII: YD01N1999R) VITAMIN A (UNII: 81G40H8B0T) VITAMIN D (UNII: 9VU1KI44GP) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM SULFITE (UNII: VTK01UQK3G) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) TRISODIUM HEDTA (UNII: K3E0U7O8KI) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CORN OIL (UNII: 8470G57WFM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-810-24 1 in 1 CARTON 1 28 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/19/2009 Labeler - CVS Pharmacy (062312574) Registrant - Pharma Pac, LLC (140807475) Establishment Name Address ID/FEI Business Operations Pharma Pac, LLC 140807475 manufacture