Label: ADULT TUSSIN- guaifenesin solution
- NDC Code(s): 69230-332-23
- Packager: Camber Consumer Care
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 20, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
Warnings
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 emphysemaWhen using this product
• do not use more than directedStop use and ask a doctor if
• cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a
serious condition.If pregnant or breast-feeding, ask a health professional before use.
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions
• do not take more than 6 doses in any 24-hour period • this adult strength product is not intended for use in children
under 12 years of age • ml = milliliter • measure only with dosing cup provided • keep dosing cup with productAge Dose Adults and Children 12 years and
over
10-20 mL every 4 hours Children under 12 years Do not use - OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- Package label: Adult Tussin Expectorant
-
INGREDIENTS AND APPEARANCE
ADULT TUSSIN
guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69230-332 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 10 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 red Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69230-332-23 1 in 1 CARTON 05/20/2025 1 237 mL 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 Drug M012 05/19/2025 Labeler - Camber Consumer Care (079539968) Registrant - Camber Consumer Care (079539968) Establishment Name Address ID/FEI Business Operations AptaPharma Inc. 790523323 manufacture(69230-332)

