Label: CONLAX- bisacodyl suppository
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NDC Code(s):
72701-102-04,
72701-102-05,
72701-102-08,
72701-102-10, view more72701-102-12, 72701-102-16, 72701-102-28, 72701-102-30
- Packager: Bliss GVS Pharma Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated March 1, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- OTHER SAFETY INFORMATION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CONLAX
bisacodyl suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72701-102 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL 10 mg Inactive Ingredients Ingredient Name Strength FAT, HARD (UNII: 8334LX7S21) Product Characteristics Color white Score Shape BULLET Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72701-102-10 2 in 1 CARTON 12/16/2018 1 5 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:72701-102-05 20 in 1 CARTON 12/16/2018 2 5 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:72701-102-04 1 in 1 CARTON 12/16/2018 3 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:72701-102-08 2 in 1 CARTON 12/16/2018 4 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:72701-102-12 3 in 1 CARTON 12/16/2018 5 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:72701-102-16 4 in 1 CARTON 12/16/2018 6 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:72701-102-28 7 in 1 CARTON 12/16/2018 7 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 8 NDC:72701-102-30 6 in 1 CARTON 03/01/2023 8 5 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 12/16/2018 Labeler - Bliss GVS Pharma Limited (675629890) Establishment Name Address ID/FEI Business Operations Bliss GVS Pharma Limited 675630493 manufacture(72701-102) , analysis(72701-102) , label(72701-102) , pack(72701-102)