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PREPARATION H

NDC 0573-2868 · Haleon US Holdings LLC

Generic nameglycerin, petrolatum, phenylephrine HCl, pramoxine HCl
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, PETROLATUM
Strength144; 150; 2.5; 10 mg/g; mg/g; mg/g; mg/g
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0573-2868-10 — 1 TUBE in 1 CARTON (0573-2868-10) / 26 g in 1 TUBE

0573-2868-20 — 1 TUBE in 1 CARTON (0573-2868-20) / 51 g in 1 TUBE

0573-2868-93 — 1 TUBE in 1 CARTON (0573-2868-93) / 26 g in 1 TUBE

0573-2868-98 — 1 TUBE in 1 CARTON (0573-2868-98) / 51 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0573-0768 — avobenzone, octinoxate, and white petrolatum, 0573-1378 — Phenylephrine hydrochloride, 0573-1912 — PETROLATUM, 0573-1921 — white petrolatum, 0573-1957 — avobenzone, homosalate, octisalate, octocrylene, white petrolatum, 0573-1958 — avobenzone, homosalate, octisalate, octocrylene, white petrolatum, 0573-2031 — camphor, menthol, petrolatum, 0573-2161 — chlorpheniramine maleate, ibuprofen, and phenylephrine hydrochloride, 0573-2840 — phenylephrine hcl, witch hazel, 0573-2843 — Glycerin, Lidocaine, Petrolatum, and Phenylephrine Hydrochloride, 0573-2871 — mineral oil, petrolatum, phenylephrine HCl, 0573-2880 — cocoa butter, phenylephrine hydrochloride, 0573-2883 — cocoa butter, phenylephrine hydrochloride, 0573-2890 — Lidocaine, Phenylephrine Hydrochloride, 0573-2919 — Phenylephrine hydrochloride, 0641-6142 — Phenylephrine Hydrochloride, 0641-6188 — Phenylephrine Hydrochloride, 0641-6189 — Phenylephrine Hydrochloride, 0641-6229 — Phenylephrine Hydrochloride, 0641-6245 — Phenylephrine Hydrochloride, +2483 more

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