CONLAX- bisacodyl suppository 
Bliss GVS Pharma Limited

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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Conlax (Bisacodyl) Suppositories

Drug Facts

Active ingredient (in each suppository)

Bisacodyl USP, 10 mg

Purpose

Stimulant Laxative

Use

Warnings

For rectal use only

Ask a doctor before use if you have

When using this product you may experience stomach discomfort, faintness, rectal burning and mild cramps

Stop use and ask a doctor if

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children

12 years of age and over

1 suppository in a single daily dose. Peel open plastic. Insert suppository

well into rectum, pointed end first. Retain about 15 to 20 minutes.

children 6 to under 12 years1/2 suppository in a single daily dose
children under 6 yearsDo not use

Other information

Inactive ingredient hard fat

Questions or Comments? 1-888-830-6075

TAMPER EVIDENT: DO NOT USE IF SEALED WRAPPER AROUND SUPPOSITORIES IS BROKEN OR MISSING

Manufactured and Marketed by:

BLISS GVS PHARMA LTD.

102, Hyde Park, Saki Vihar Road,

Andheri (E), Mumbai - 400 072, INDIA

Email: info@blissgvs.com

www.blissgvs.com

Bliss GVS

NDC 72701-102-10

Conlax 10MG

Bisacodyl USP, 10 mg

Stimulant Laxative

Gentle, Predictable, Fast Relief

10 suppositories

DO NOT SWALLOW

CONLAX_Supps(10ct)

CONLAX 
bisacodyl suppository
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72701-102
Route of AdministrationRECTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL10 mg
Inactive Ingredients
Ingredient NameStrength
FAT, HARD (UNII: 8334LX7S21)  
Product Characteristics
ColorwhiteScore    
ShapeBULLETSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72701-102-102 in 1 CARTON12/16/2018
15 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:72701-102-0520 in 1 CARTON12/16/2018
25 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:72701-102-041 in 1 CARTON12/16/2018
34 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:72701-102-082 in 1 CARTON12/16/2018
44 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:72701-102-123 in 1 CARTON12/16/2018
54 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:72701-102-164 in 1 CARTON12/16/2018
64 in 1 BLISTER PACK; Type 0: Not a Combination Product
7NDC:72701-102-287 in 1 CARTON12/16/2018
74 in 1 BLISTER PACK; Type 0: Not a Combination Product
8NDC:72701-102-306 in 1 CARTON03/01/2023
85 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33412/16/2018
Labeler - Bliss GVS Pharma Limited (675629890)
Establishment
NameAddressID/FEIBusiness Operations
Bliss GVS Pharma Limited675630493manufacture(72701-102) , analysis(72701-102) , label(72701-102) , pack(72701-102)

Revised: 3/2023
Document Id: f655d8d8-cc78-713b-e053-2995a90af916
Set id: 7d25990b-6f7c-1eac-e053-2a91aa0a7022
Version: 2
Effective Time: 20230301
 
Bliss GVS Pharma Limited