MEDIQUE DIOTAME- bismuth subsalicylate tablet, chewable 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Medique Diotame

Drug Facts

Active ingredient (in each tablet)

Bismuth Subsalicylate 262 mg

(each tablet contains 102 mg salicylate)

Purpose

Upset stomach reliever/antidiarrheal

Uses

relieves

  • traveler's diarrhea
  • diarrhea
  • upset stomach reliever due to overindulgence in food and drink, including:
  • heartburn
  • indigestion
  • nausea
  • gas
  • belching
  • fullness

Warnings

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's Syndrome a rare but serious illness.

Allergy alert: Contains salicylate. Do not take if you are:

  • allergic to salicylates (including aspirin)
  • taking other salicylate products

Do not use if you have

  • bloody or black stool
  • an ulcer
  • a bleeding problem

Ask a doctor before use if you have

  • fever
  • mucus in the stool

Ask a doctor or pharmacist if you are taking any other drug for

  • anticoagulation (thinning of the blood)
  • diabetes
  • gout
  • arthritis

When using this product a temporary and harmless darkening of the tongue and/or stool may occur.

Stop use and ask a doctor if

  • symptoms get worse
  • ringing in the ears or loss of hearing occurs
  • diarrhea lasts more than 2 days

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

Keep out of reach of children. In case of accidental overdose, contact a physician or poison control center immediately (1-800-222-1222).

Directions

  • chew or dissolve in mouth
  • do not swallow tablets whole
  • drink plenty of clear fluids to help prevent dehydration, which may accompany diarrhea

Adults and children: (12 years and older)

  • chew 2 tablets every 1/2 to 1 hour as needed
  • do not exceed 16 tablets in 24 hours
  • use until diarrhea stops but not more than 2 days

​Children under 12 years:

ask a doctor

Other information

  • phenylketonurics: contains phenylalanine 1.1mg per tablet
  • each tablet contains 73mg elemental calcium
  • store at room temperature 59°-86°F (15°-30°C)
  • tamper-evident sealed packets
  • do not use any opened or torn packets

Inactive ingredients

acacia gum, aspartame, calcium carbonate, D&C red #27, dextrates, flavoring, magnesium stearate, maltodextrin, microcrystalline cellulose, peppermint flavor, silicon dioxide

Questions or comments? 1-800-634-7680

Medique Diotame Label

Medique®

Diotame

Chewable Tablets

Chew or crush tablets completely before swallowing

Do not swallow tablets whole

Pull To Open

Upset Stomach/Diarrhea • Bismuth Subsalicylate 262 mg

100 Tablets

(50 x 2)

Tamper Evident Unit Dose Packets

220T Medique

MEDIQUE DIOTAME 
bismuth subsalicylate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-210
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ, BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE262 mg
Inactive Ingredients
Ingredient NameStrength
ASPARTAME (UNII: Z0H242BBR1)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
D&C RED NO. 27 (UNII: 2LRS185U6K)  
DEXTRATES (UNII: G263MI44RU)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
ACACIA (UNII: 5C5403N26O)  
Product Characteristics
ColorpinkScoreno score
ShapeROUNDSize16mm
FlavorImprint Code RH;046
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-210-8315 in 1 BOX04/01/2014
1NDC:47682-210-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-210-3350 in 1 BOX04/01/2014
22 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-210-13250 in 1 BOX04/01/2014
32 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-210-6412 in 1 BOX04/01/2014
42 in 1 PACKET; Type 0: Not a Combination Product
5NDC:47682-210-992 in 1 PACKET; Type 0: Not a Combination Product04/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33504/01/2014
Labeler - Unifirst First Aid Corporation (832947092)
Establishment
NameAddressID/FEIBusiness Operations
Prestige Packaging080667761relabel(47682-210) , repack(47682-210)

Revised: 5/2021
 
Unifirst First Aid Corporation