AKIN COUGH FORMULA DM STRAWBERRY BANANA- dextromethorphan hydrobromide, guaifenesin liquid 
Southern Sales & Service, Inc.

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Akin Cough Formula DM (Strawberry - Banana)

Drug Facts

Active ingredient (in each 5ml tsp.)

Dextromethorphan HBr USP 10 mg

Guaifenesin USP 100 mg

Purpose

Cough suppressant

Expectorant

Uses

• temporarily quiets cough associated with the common cold or inhaled irritants • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.

Warnings

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 you are taking a prescription drug that contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if

• you have a cough that lasts or a chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema • cough occurs with too much phlegm (mucus)

Stop use and ask a doctor if

• cough lasts for more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

If pregnant or beast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Do not take more than 6 doses in any 24 hours period

Adults and children 12 years and over10 ml (2 teaspoonfuls every 4 hours or as directed by doctor)
Children under 12 yearsdo not use

Other information

• store at room temperature • 15°-30°C (59°-86°F)

Do not use if seal under cap is torn, broken or missing. TAMPER-EVIDENT:

Inactive ingredients

Citric acid, FD&C red #40, glycerin, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, sodium citrate, strawberry-banana flavor, sucralose.

Package Labeling:

Label0

AKIN COUGH FORMULA DM STRAWBERRY BANANA 
dextromethorphan hydrobromide, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-211
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69822-211-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01202/01/2023
Labeler - Southern Sales & Service, Inc. (013114906)

Revised: 11/2023
Document Id: 0b57d80b-329c-212b-e063-6394a90a4e18
Set id: 7a81efd8-775d-455e-860f-f3e3b369a0a7
Version: 2
Effective Time: 20231129
 
Southern Sales & Service, Inc.