Label: MAXIMUM STRENGTH GAS RELIEF- simethicone capsule, liquid filled
- NDC Code(s): 51013-127-04, 51013-127-22
- Packager: PURACAP PHARMACEUTICAL LLC
- Category: HUMAN OTC DRUG LABEL
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 December 20, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each softgel)
- Purpose
- Use
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL - 24ct
- PRINCIPAL DISPLAY PANEL - 60ct
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INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH GAS RELIEF
simethicone capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51013-127 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 250 mg Inactive Ingredients Ingredient Name Strength D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Product Characteristics Color purple Score no score Shape capsule (oval) Size 13mm Flavor Imprint Code PC31 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51013-127-04 2 in 1 CARTON 01/11/2016 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:51013-127-22 1 in 1 CARTON 01/11/2016 2 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part332 01/11/2016 Labeler - PURACAP PHARMACEUTICAL LLC (962106329) Establishment Name Address ID/FEI Business Operations Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd. 421293287 manufacture(51013-127) , analysis(51013-127)