Label: GERI-TUSSIN EXPECTORANT- guaifenesin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 17856-0793-1, 17856-0793-2, 17856-0793-3 - Packager: Atlantic Biologicals Corps
- This is a repackaged label.
- Source NDC Code(s): 57896-793
- 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 June 20, 2018
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (per teaspoonful = 5mL)
- Purpose
- Uses
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Warnings
Do not use if you are hypersensitive to any of the ingredients
Ask a doctor before use if you have
- cough that occurs with too much phlegm (mucus)
- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
Stop use and ask a doctor ifcough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
- Directions
- Other information
- Inactive ingredients
- HOW SUPPLIED
- GERI-TUSSIN EXPECTORANT (GUAIFENESIN) LIQUID
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INGREDIENTS AND APPEARANCE
GERI-TUSSIN EXPECTORANT
guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17856-0793(NDC:57896-793) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CARAMEL (UNII: T9D99G2B1R) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM BENZOATE (UNII: OJ245FE5EU) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) WATER (UNII: 059QF0KO0R) Product Characteristics Color red Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17856-0793-1 15 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product 05/02/2018 2 NDC:17856-0793-2 10 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product 05/02/2018 3 NDC:17856-0793-3 5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product 05/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 01/01/2000 Labeler - Atlantic Biologicals Corps (047437707) Establishment Name Address ID/FEI Business Operations Atlantic Biologicals Corps 047437707 RELABEL(17856-0793) , REPACK(17856-0793)