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Benzocaine

NDC 71888-101 · Bellus Medical, LLC

Generic nameBenzocaine
Dosage formGEL
RouteTOPICAL
Active ingredient(s)BENZOCAINE
Strength200 mg/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

71888-101-02 — 12 PACKET in 1 BOX (71888-101-02) / 4 mL in 1 PACKET (71888-101-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71363-105 — Benzocaine, 71363-106 — Benzocaine, 71363-107 — Benzocaine, 71584-0109 — BENZOCAINE, ALCOHOL, 71683-004 — Benzocaine, 71683-005 — Benzocaine, 71687-1053 — Benzocaine, 71730-009 — benzocaine wipes, 71734-113 — Benzocaine, 71734-340 — Benzocaine and Isopropyl Alcohol, 71922-100 — Benzocaine, 71922-101 — Benzocaine, 71922-102 — Benzocaine, 71922-103 — Benzocaine, 71922-104 — Benzocaine, 71922-105 — Benzocaine, 72459-013 — BENZOCAINE, ISOPROPYL ALCOHOL, 72459-016 — BENZOCAINE, ISOPROPYL ALCOHOL, 72459-022 — BENZOCAINE, 72484-433 — Benzocaine, +563 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.