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Hemorroidal Cooling gel

NDC 68016-054 · Pharmacy Value Alliance, LLC

Generic namePhenylephrine, Witch Hazel
Dosage formGEL
RouteTOPICAL
Active ingredient(s)WITCH HAZEL, PHENYLEPHRINE HYDROCHLORIDE
Strength.25; .5 g/100g; g/100g
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

68016-054-09 — 1 TUBE in 1 BOX (68016-054-09) / 26 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67091-471 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 67091-691 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 67172-503 — Phenylephrine hydrochloride and Glycerin, 67414-402 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 67414-507 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 67751-149 — CHLORPHENIRAMINE MALEATE, IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-150 — IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-217 — chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, 67751-239 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 67751-240 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 68016-154 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 68016-322 — Cocoa Butter, Phenylephrine HCl, 68016-528 — Mineral Oil, Petrolatum, Phenylephrine HCI, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68047-129 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-143 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-186 — Chlorpheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68083-338 — phenylephrine hydrochloride, 68083-339 — phenylephrine hydrochloride, +1632 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.