INSTARELIEF NIGHTTIME SLEEP AID- diphenhydramine hydrochloride liquid 
DXM Pharmacuetical, Inc.

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Active ingredient

(in each 3mL) (one dose) Diphenhydramine HCI, 50 mg

Purpose

Nighttime sleep-aid

Uses

Warning

Do not use

Do not take this product, unless directed by a doctor

Do not take this product ifyou are taking sedatives or tranquilizers, without first consulting your doctor. Avoid alcoholic beverages while taking this product. If sleeplessness persists continuously for more than 2 weeks, consult your doctor. Insomnia may be a symptom of serious underlying medical illness.


If pregnant or breast-feeding, ask a doctor before use.


Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

​Directions

agedose
adults and children 12 years and over

3mL at bedtime

children under 12 yearsdo not use

Other information 

TAMPER EVIDENT: Do not use if seal on the bottle is broken.
store at 20-25°C (68-77°F). Do not refrigerate.

Inactive ingredients

citric acid, glycerin, grape flavor, propylene glycol, purified water, sodium benzoate, sodium citrate, stevia, sucralose, sucrose

Questions or comments?

Call 1-833-289-7626 between 10 a.m. to 4 p.m. CST, Monday through Friday or visit our website www.InstaRelief.com to report serious adverse events associated with the use of this product. Please call a doctor for medical advice.

Product label

image description
INSTARELIEF NIGHTTIME SLEEP AID 
diphenhydramine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71598-120
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg  in 3 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
STEVIA LEAF (UNII: 6TC6NN0876)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71598-120-191 in 1 CARTON10/01/2023
1120 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01010/01/2023
Labeler - DXM Pharmacuetical, Inc. (080748277)
Registrant - DXM Pharmacuetical, Inc. (080748277)

Revised: 12/2023
Document Id: 0cf37e8d-75f6-6dfb-e063-6294a90a8280
Set id: e0459e71-32dd-4715-b103-bb14db42c5f3
Version: 1
Effective Time: 20231220
 
DXM Pharmacuetical, Inc.