Respiratory & Allergy

Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine HydrochlorideThird Party Manufacturing in India

Looking to get Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
93-14-1 (Guaifenesin), 147-24-0 (Diphenhydramine HCl), 3572-43-8 (Bromhexine), 154-41-6 (Phenylpropanolamine HCl)
Drug Class
Expectorant + Antihistamine + Mucolytic + Decongestant combination
Molecular Formula
C₁₀H₁₄O₄ (Guaifenesin) + C₁₇H₂₂ClNO (Diphenhydramine HCl) + C₁₄H₂₀Br₂N₂ (Bromhexine) + C₉H₁₄ClNO (Phenylpropanolamine HCl)
Molecular Weight
Combination product
Grade Standards
IP, BP, USP
Therapeutic Category
Respiratory & Allergy
MOQ
Contact us for MOQ — varies by strength and dosage form
Dosage Forms
Syrup

Mechanism of Action

This quad-combination syrup works through four complementary pharmacological actions to provide comprehensive symptomatic relief from cough, congestion, and upper respiratory discomfort. Guaifenesin acts as an expectorant by increasing the volume and reducing the viscosity of bronchial secretions through stimulation of vagal nerve endings in the gastric mucosa. This reflex enhances the production of thinner, less tenacious mucus that is more easily cleared by productive cough, improving airway patency and mucociliary clearance. Diphenhydramine Hydrochloride is a first-generation antihistamine that competitively blocks histamine H1 receptors, suppressing histamine-mediated allergic responses including sneezing, rhinorrhea, nasal pruritus, and bronchospasm. Its central anticholinergic activity further contributes to its antitussive effect by elevating the cough threshold in the medullary cough center. Bromhexine functions as a mucolytic agent by depolymerizing acid mucopolysaccharide fibers within bronchial secretions, breaking down thick, viscid sputum into thinner, less cohesive material that is easier to expectorate. Phenylpropanolamine Hydrochloride exerts its decongestant action through direct stimulation of alpha-1 adrenergic receptors in the nasal and respiratory mucosa, producing vasoconstriction that reduces tissue edema, nasal congestion, and sinus pressure while restoring upper airway patency.

Therapeutic Uses & Indications

Therapeutic Uses

This combination syrup is indicated for the symptomatic relief of cough and respiratory congestion associated with common cold, allergic rhinitis, and upper respiratory tract infections:

  • Productive Cough with Congestion: Loosens thick mucus while reducing nasal congestion, allowing patients to clear secretions more effectively
  • Allergic Rhinitis with Cough: Addresses both histamine-mediated nasal symptoms and associated cough through the combined action of antihistamine and expectorant
  • Acute Bronchitis: Provides symptomatic relief from cough, chest congestion, and associated nasal obstruction during acute episodes
  • Sinusitis: Reduces nasal mucosal edema and promotes drainage of the paranasal sinuses while managing post-nasal drip-induced cough

Why Manufacturers Choose Guaifenesin + Diphenhydramine + Bromhexine + Phenylpropanolamine

This quad-combination formulation occupies a strong position in the Indian cough and cold market, where combination products are widely prescribed for comprehensive symptom relief. The syrup formulation is particularly popular in the paediatric and geriatric segments, where multi-symptom cough preparations are a mainstay of treatment. The combination addresses all major cough and cold symptoms—expectoration, antihistamine action, mucolysis, and decongestion—within a single product, reducing the need for polypharmacy.

For manufacturers, this formulation offers clear advantages in the PCD franchise segment, where differentiated combination products command better margins than single-molecule cough syrups. All four APIs are readily available from domestic suppliers, and the formulation process for oral liquids is well established in Indian WHO-GMP facilities. The product enjoys steady year-round demand that spikes during seasonal respiratory illness peaks, providing both consistent baseline volume and seasonal upside. It is also well suited for institutional supply to hospitals and nursing homes that stock comprehensive cough and cold ranges.

This makes this combination one of the most sought-after formulations for third party manufacturing in India, with consistent demand from PCD franchise operators and export-oriented companies.

Dosage Forms We Manufacture

Syrup
50mg + 10mg + 4mg + 7.5mg per 10ml

Frequently Asked Questions

What is the minimum order quantity for Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride?
Minimum order quantity for Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride is Contact us for MOQ — varies by strength and dosage form. Please contact us for bulk pricing and custom quantities.
What dosage forms of Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride can you manufacture?
We manufacture Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride as: Syrup (50mg + 10mg + 4mg + 7.5mg per 10ml).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride for export?
Yes. We provide export-ready Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride?
We manufacture Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride to IP, BP, USP pharmacopoeial standards.
Third Party Manufacturing

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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

PET bottle, HDPE bottle with child-resistant cap, Glass bottle. Packaging customized to client brand guidelines.

Start Manufacturing Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Guaifenesin + Diphenhydramine Hydrochloride + Bromhexine + Phenylpropanolamine Hydrochloride across all dosage forms. PCD franchise and export orders welcome.

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