Label: DEXTROMETHORPHAN HYDROBROMIDE capsule, liquid filled
- NDC Code(s): 68210-0106-1, 68210-0106-2, 68210-0106-3
- Packager: Spirit Pharmaceuticals 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.
Updated March 16, 2020
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- SPL UNCLASSIFIED SECTION
- Active ingredient (in each softgel)
Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product
Ask a doctor before use if you have
- a cough that occurs with too much phlegm (mucus)
- a cough that lasts or is chronic as occurs with smoking, asthma, or emphysema
Stop use and ask doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
dextromethorphan hydrobromide capsule, liquid filled
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68210-0106 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POVIDONE K30 (UNII: U725QWY32X) GLYCERIN (UNII: PDC6A3C0OX) GELATIN (UNII: 2G86QN327L) SORBITOL (UNII: 506T60A25R) FD&C RED NO. 40 (UNII: WZB9127XOA) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color red Score no score Shape OVAL Size 13mm Flavor Imprint Code 404 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68210-0106-1 1 in 1 CARTON 04/10/2018 1 15 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:68210-0106-2 1 in 1 CARTON 03/12/2020 2 240 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:68210-0106-3 1 in 1 CARTON 03/12/2020 3 60 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 04/10/2018 Labeler - Spirit Pharmaceuticals LLC (179621011) Establishment Name Address ID/FEI Business Operations MEDGEL PVT LTD 677385498 manufacture(68210-0106)