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Medi Fect

NDC 12745-177 · Medical Chemical Corporation

Generic nameEthyl Alcohol
Dosage formLIQUID
RouteTOPICAL
Active ingredient(s)ALCOHOL, DIAZOLIDINYL UREA
Strength59.86; 1 g/100mL; g/100mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

12745-177-01 118 mL in 1 BOTTLE, PLASTIC (12745-177-01)

12745-177-02 473 mL in 1 BOTTLE, PLASTIC (12745-177-02)

12745-177-03 3785 mL in 1 BOTTLE, PLASTIC (12745-177-03)

12745-177-04 18927 mL in 1 BOTTLE, PLASTIC (12745-177-04)

12745-177-05 59 mL in 1 BOTTLE, PLASTIC (12745-177-05)

12745-177-06 237 mL in 1 BOTTLE, PLASTIC (12745-177-06)

12745-177-07 946 mL in 1 BOTTLE, PLASTIC (12745-177-07)

12745-177-08 208198 mL in 1 DRUM (12745-177-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-867 — ALCOHOL, 11673-868 — ALCOHOL, 11673-869 — ALCOHOL, 11673-870 — ALCOHOL, 11701-025 — Alcohol, 11822-0023 — Ethyl Alcohol, 11822-3700 — Alcohol, 11822-6450 — Ethyl Alcohol, 11928-004 — Alcohol, 11928-005 — Alcohol, 12745-180 — Ethyl Alcohol, 15127-008 — Ethyl alcohol, 15127-009 — Ethyl alcohol, 16729-710 — ALCOHOL, 17518-050 — Alcohol, 17518-051 — Chlorhexidine Gluconate and Alcohol, 21130-066 — Alcohol, 21130-068 — Alcohol, 21130-077 — Alcohol, 21749-022 — ALCOHOL, +2737 more

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