Label: TUSSIN EXPECTORANT- guaifenesin liquid
- NDC Code(s): 68016-020-04, 68016-020-08
- Packager: Chain Drug Consortium, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 29, 2023
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- Active ingredient
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Directions
- Other information
- Inactive ingredients
- Questions?
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Product Label
NDC 68016-020-04
Premier Value®
TussinGuaifenesin Oral solution, USP
EXPECTORANT
Relieves Chest Congestion
Loosens Mucus
Non-DrowsyAdult
For ages 12 and OverCherry Flavor Liquid
8 FL OZ (37 mL)
INDEPENDENTLY TESTED SATISFACTION GUARANTEED PV
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSINGIf for Any reason you are not satisfied with this product, lease return it to the store where purchased for a full refund.
DISTRIBUTED BY
CHAIN DRUG CONSORTIUM
3301 NW BOCA RATON BLVD
SUITE 101, BOCA RATON, FL 33431BX-016
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INGREDIENTS AND APPEARANCE
TUSSIN EXPECTORANT
guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-020 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 CARAMEL (UNII: T9D99G2B1R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) DEXTROSE (UNII: IY9XDZ35W2) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) MENTHOL (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) Product Characteristics Color Score Shape Size Flavor CHERRY (cherryFlavor Liquid) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-020-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/07/2012 2 NDC:68016-020-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/07/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 09/07/2012 Labeler - Chain Drug Consortium, LLC (101668460) Registrant - AptaPharma, Inc. (790523323) Establishment Name Address ID/FEI Business Operations AptaPharma, Inc. 790523323 manufacture(68016-020)