Label: SUNMARK GAS RELIEF- dimethicone tablet, chewable
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Contains inactivated NDC Code(s)
NDC Code(s): 49348-509-07 - Packager: McKesson
- 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 April 10, 2014
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Warnings
- Directions
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SUNMARK GAS RELIEF
dimethicone tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-509 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg Inactive Ingredients Ingredient Name Strength RAW SUGAR (UNII: 8M707QY5GH) DEXTROSE (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SORBITOL (UNII: 506T60A25R) Product Characteristics Color white Score no score Shape ROUND Size 14mm Flavor PEPPERMINT Imprint Code GDC156 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49348-509-07 3 in 1 CARTON 1 12 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part332 04/10/2004 Labeler - McKesson (177667227)