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NDC 11673-0186-40 Up and Up Nighttime Sleep Aid 50 mg/30mL Details

Up and Up Nighttime Sleep Aid 50 mg/30mL

Up and Up Nighttime Sleep Aid is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is DIPHENHYDRAMINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is also used to relieve cough caused by minor throat or airway irritation. Diphenhydramine is also used to prevent and treat motion sickness, and to treat insomnia (difficulty falling asleep or staying asleep). Diphenhydramine is also used to control abnormal movements in people who have early stage parkinsonian syndrome (a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) or who are experiencing movement problems as a side effect of a medication. Diphenhydramine will relieve the symptoms of these conditions but will not treat the cause of the symptoms or speed recovery. Diphenhydramine should not be used to cause sleepiness in children. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.

Related Packages: 11673-0186-40
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Diphenhydramine

Product Information

NDC	11673-0186
Product ID	11673-186_a2d146f9-2a18-4528-aeb3-74061bc95375
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Up and Up Nighttime Sleep Aid
Proprietary Name Suffix	n/a
Non-Proprietary Name	diphenhydramine hydrochloride
Product Type	HUMAN OTC DRUG
Dosage Form	SOLUTION
Route	ORAL
Active Ingredient Strength	50
Active Ingredient Units	mg/30mL
Substance Name	DIPHENHYDRAMINE HYDROCHLORIDE
Labeler Name	Target Corporation
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part338
Listing Certified Through	2024-12-31

Package

NDC 11673-0186-40 (11673018640)

Pricing Information	N/A
NDC Package Code	11673-186-40
Billing NDC	11673018640
Package	355 mL in 1 BOTTLE (11673-186-40)
Marketing Start Date	2020-03-26
NDC Exclude Flag	N