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Premier Value Milk of Magnesia

NDC 68016-850 · Pharmacy Value Alliance, LLC

Generic nameMagnesium Hydroxide
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)MAGNESIUM HYDROXIDE
Strength80 mg/mL
Pharmacologic classCalculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

68016-850-16 — 473 mL in 1 BOTTLE, PLASTIC (68016-850-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63941-649 — magnesium hydroxide, 65197-300 — Alumina, Magnesia, Simethicone, 66715-6422 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-6522 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-7822 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 66715-9822 — Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet, 67618-102 — Magnesium hydroxide, 67751-202 — Famotidine, Calcium carbonate, and Magnesium hydroxide, 68016-678 — Calcium Carbonate ,Magnesium Hydroxide, 68016-679 — Calcium carbonate ,Magnesium hydroxide,Simethicone, 68071-3423 — aluminum hydroxide, magnesium hydroxide, dimethicone, 68071-4114 — aluminum hydroxide, magnesium hydroxide, dimethicone, 68071-5289 — aluminum hydroxide, magnesium hydroxide, dimethicone, 68788-7841 — aluminum hydroxide, magnesium hydroxide, dimethicone, 68788-8169 — aluminum hydroxide, magnesium hydroxide, dimethicone, 68788-8506 — aluminum hydroxide, magnesium hydroxide, simethicone, 68788-8638 — magnesium hydroxide, 69256-503 — aluminum hydroxide, magnesium hydroxide, simethicone, 69256-508 — aluminum hydroxide, magnesium hydroxide, simethicone, 69256-517 — aluminum hydroxide, magnesium hydroxide, simethicone, +280 more

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