Akin Solution
FDA Label NDC 69822-200

12 label sections · Submitted to the FDA by Southern Sales & Service, Inc. · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Southern Sales & Service, Inc. for the product Akin (NDC 69822-200). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, (in each 5ml tsp.) active ingredient, purpose, uses, warnings, stop use, and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

(In Each 5Ml Tsp.) Active Ingredient

Guaifenesin USP 100 mg

Purpose

Expectorant

Warnings

Do not take this product for persistent or chronic couch such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or where cough is accompanied by excessive phlegm(mucus) unless directed by a doctor."

Stop Use

And Ask A Doctor If

cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache, consult a doctor. A persistent cough may be a sign of a serious condition.

If Pregnant Or Breast-Feeding,

ask a health professional before use.

Keep Out Of The Reach Of Children.

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

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

Propylene glycol, glycerine, citric acid, sucralose, sodium citrate, potasium sorbate, methylparaben, propylparaben, cherry flavor, menthol, FD &C Red # 40, caramel color, purified water.

* Please review the disclaimer below.