Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Packaging of Lotions

Posted on By

SOP for Packaging of Lotions

Standard Operating Procedure for Lotion Packaging

1) Purpose

The purpose of this SOP is to outline the standardized procedure for the packaging of lotions to ensure the integrity, safety, and quality of the final product.

2) Scope

This SOP applies to all personnel involved in the packaging process of lotions within the pharmaceutical manufacturing facility.

3) Responsibilities

The responsibilities for executing this SOP are as follows:

Packaging Operators:

  • Carry out the packaging process as per the SOP.
  • Ensure packaging materials are suitable and meet quality standards.

Quality Control Personnel:

  • Inspect and verify the quality of the packaged product and packaging materials.
  • Ensure compliance with packaging specifications and standards.
See also  SOP for Stability Testing of Lotions

Packaging Supervisors:

  • Oversee the packaging process to ensure adherence to the SOP and resolve any issues.

4) Procedure

4.1 Pre-Operational Checks:

  • Ensure the packaging area is clean and sanitized.
  • Verify the availability and condition of packaging materials (bottles, labels, caps, etc.).
  • Ensure all packaging equipment is clean, calibrated, and in good working order.

4.2 Packaging Process:

  1. Filling:
    1. Set up the filling machine according to the specified volume for the lotion.
    2. Ensure the lotion is at the correct temperature and homogeneity before filling.
    3. Fill the lotion into the containers as per the specified volume.
  2. Sealing:
    1. Place caps or seals on the filled containers securely.
    2. Verify that the seals are intact and free from defects.
  3. Labeling:
    1. Label each container with the appropriate product label, including batch number, expiration date, and other required information.
    2. Ensure labels are applied straight and adhere firmly to the containers.
  4. Inspection:
    1. Inspect the packaged product for any defects or inconsistencies.
    2. Remove any non-conforming products from the packaging line.
  5. Cartoning:
    1. Place labeled containers into cartons or boxes as per the packaging plan.
    2. Ensure cartons are sealed properly and labeled with batch details.
  6. Storage:
    1. Transfer the packaged products to the designated storage area.
    2. Store products under appropriate conditions as specified (e.g., temperature, humidity).
See also  SOP for Process Optimization for Lotions

4.3 Post-Operational Activities:

  • Document the packaging activities in the batch record.
  • Clean the packaging equipment and area according to the cleaning SOP.

5) Abbreviations, if any

None.

6) Documents, if any

  • Batch Packaging Record
  • Equipment Logbook
  • Cleaning Record

7) Reference, if any

  • Good Manufacturing Practice (GMP) guidelines
  • FDA Packaging Guidelines

8) SOP Version

Version 1.0

Lotions Tags:Analytical method development for lotions, Calibration of equipment for lotions, Cleaning of equipment for lotions, disposal of waste in lotion production, Documentation in lotion production, Emulsification process in lotions, Homogeneity testing in lotions, In-process testing for lotions, Lotion batch testing, Lotion production SOP, Lotion testing procedures, Microbial testing for lotions, Particle size analysis in lotions, pH testing in lotions, Preventing contamination in lotion production, Process validation for lotions, Quality control for lotions, Quality testing for lotions, Raw material inspection for lotions, Rheological testing for lotions, Sample collection for lotions, SOP for lotion manufacturing, Stability testing for lotions, Training personnel for lotion manufacturing, Viscosity testing in lotions

Post navigation

Previous Post: SOP for Safety Data Sheet (SDS) Management for Aerosols
Next Post: SOP for Regulatory Submission for Transdermal Patches

Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version