NYTOL- diphenhydramine hcl capsule, gelatin coated 
Medtech Products Inc.

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Nytol Gelcap 50 mg_Export only 63029-928

Drug Facts

Active ingredient

Purpose

Diphenhydramine Hydrochloride 50 mg             Nighttime sleep aid

  

Uses/ Indications

● helps to reduce difficulty falling asleep

● relieves occasional sleeplessness

Warnings

Do not use

  • if you are elderly, as this drug may cause excitation rather than sedation
  • with any other product containing diphenhydramine, even one used on skin
  • in children under 12 years of age

Ask a doctor or pharmacist before use if you

  • have
    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma
  • difficulty urinating
  • take sedatives or tranquilizers
  • are pregnant or breast-feeding

When using this product

avoid drinking alcohol

Stop use and ask a doctor if

sleeplessness continues for more than 2 weeks. Sleeplessness may be a symptom of a serious underlying medical illness.

Keep out of reach of children.

In case of overdose, call a poison control centre or get medical help right away.

Directions

Adults and children 12 years and over:

take 1 capsule at bedtime if needed, or as directed by a doctor

Other information

Store between 15 & 30 °C

Inactive ingredients

edible white ink, FD&C blue #1, gelatin, glycerin, polyethylene glycol, purified water, sorbitol sorbitan

Questions?

1-800-465-8811 www.nytol.ca

PRINCIPAL DISPLAY PANEL

Extra Strength Ultra-fort

Nytol®/MD

QUICKGELS®

GÉLULES-RAPIDESMC

Extra Strength Ultra-fort

50 mg Diphenhydramine Hydrochloride Capsules USP

Capsules de chlorhydrate de diphenhydramine 50 mg USP

16 soft gels

gélules molles

DIN 02237169

PRINCIPAL DISPLAY PANEL
Extra Strength Ultra-fort
Nytol®/MD

QUICKGELS®
GÉLULES-RAPIDESMC
Extra Strength Ultra-fort
50 mg Diphenhydramine Hydrochloride Capsules USP 
Capsules de chlorhydrate de diphenhydramine 50 mg USP 

16 soft gels 
gélules molles

DIN 02237169

NYTOL 
diphenhydramine hcl capsule, gelatin coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-928
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SORBITAN (UNII: 6O92ICV9RU)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorblueScoreno score
ShapeOVALSize1mm
FlavorImprint Code N
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-928-162 in 1 CARTON06/01/2012
18 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Export only06/01/2012
Labeler - Medtech Products Inc. (122715688)

Revised: 1/2024
Document Id: 5d247606-d3d7-4750-838f-40e09b5567f3
Set id: fc3d981c-313c-49f6-b7ee-5524ee6ef056
Version: 2
Effective Time: 20240119
 
Medtech Products Inc.