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If pregnant or breast-feeding , ask a health professional before use. Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions ▪ take only one dose per day (24 hours) – see Overdose warning ▪ measure with dosing cup provided. One Dose = 30 mL (2 tablespoons) at bed time if needed or as directed by a doctor. Other information ▪ each 30 mL dose (2 tablespoons) contains: sodium 23 mg ▪ store at room temperature ▪ protect from light. anhydrous citric acid, FD&C blue 1, FD&C red 40, flavor, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum. Compare to the active ingredient in ZzzQuil® Nighttime Sleep-Aid* Not for treating cold or flu. FAILURE TO FOLLOW THESE WARNINGS COULD RESULT IN SERIOUS CONSEQUENCES. TAMPER EVIDENT: DO NOT USE IF PRINTED SHRINK BAND IS MISSING OR BROKEN. *This product is not manufactured or distributed by Procter & Gamble, the distributor of ZzzQuil® Nighttime Sleep Aid Softgels. Dosage form: capsule, gelatin coated Ingredients: Diphenhydramine Hydrochloride 25mg Labeler: CVS Pharmacy,Inc.

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Active ingredient (in each softgel) Diphenhydramine HCl 25 mg. Uses • for the relief of occasional sleeplessness • reduces time to fall asleep if you have difficulty falling asleep. • for children under 12 years of age • with any other product containing diphenhydramine, even one used on skin. • with other drugs that cause drowsiness such as antihistamines and nighttime cold/flu products. • a breathing problem such as asthma, emphysema, or chronic bronchitis • glaucoma • difficulty in urination due to enlargement of the prostate gland • heart disease. Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers or any other sleep- aid. • avoid alcoholic beverages and other drugs that cause drowsiness • drowsiness will occur • be careful when driving a motor vehicle or operating machinery. Stop use and ask a doctor if sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding , ask a health professional before use. Overdose warning: Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Directions • take only one dose per day (24 hours) - see Overdose warning. One Dose = TWO 25 mg Softgels (50 mg) at bedtime if needed or as directed by a doctor. Other information • store at 20-25° C (68-77° F) • avoid excessive heat above 40°C (104° F) and high humidity • protect from light. FD&C blue 1, FD&C red 40, gelatin, glycerin, methyl paraben, polyethylene glycol, propyl paraben, purified water, sorbitol, titanium dioxide. Compare to the active ingredient in ZzzQuil LiquiCaps ® * Non- habit forming softgels. Failure to follow these warnings could result in serious consequences. TAMPER EVIDENT: THIS PACKAGE IS SAFETY SEALED & CHILD RESISTANT. *This product is not manufactured or distributed by Proctor & Gamble, the distributor of ZzzQuil ® LiquiCaps ® . NIGHTTIME SLEEP AID SOFTGELS diphenhydramine hydrochloride capsule, gelatin coated. Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-889 Route of Administration ORAL DEA Schedule.

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Diphenhydramine Hydrochloride (Diphenhydramine) Diphenhydramine Hydrochloride 25 mg. Inactive Ingredients Ingredient Name Strength FD&C Blue No.

40 gelatin glycerin METHYLPARABEN polyethylene glycols PROPYLPARABEN water sorbitol titanium dioxide. Product Characteristics Color PURPLE Score no score Shape CAPSULE Size 15mm Flavor Imprint Code 060;R060 Contains. Packaging # Item Code Package Description 1 NDC:69842-889-48 4 BLISTER PACK in 1 CARTON 1 12 CAPSULE, GELATIN COATED in 1 BLISTER PACK. Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part338 07/14/2015. (062312574) Use these dosage charts for infants and children under 12 years old: Gimoti (metoclopramide) is an intranasal formulation of the approved drug.

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