- Active Ingredient
- Purpose
- Uses
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Warnings
Allergy alert Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "-caine" anesthetics.
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- Distributed by
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MARK 3
benzocaine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61509-102 Route of Administration ORAL, DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 6.4 g in 32 g Inactive Ingredients Ingredient Name Strength FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) SACCHARIN SODIUM (UNII: SB8ZUX40TY) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XYLITOL (UNII: VCQ006KQ1E) Product Characteristics Color Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61509-102-32 32 g in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 02/28/2014 Labeler - Cargus International, Inc. (096191093) Establishment Name Address ID/FEI Business Operations Dharma Research, Inc. 078444642 manufacture(61509-102)