Irish Sea Moss Powder

Latine name: Chondrus crispus
specification:/
Solvent used: No Solvent Used
Appearance: Fine White to light yellow
Plant Part Used: Whole
Package: 25kgs/drum
MOQ: 25kgs
Sample: Free Sample is available
Lead time: In stock, 2nd day picking up
Certificates:NSF GMP, Kosher, Halal, ISO,FSSC22000,Organic
Product Description

Irish Sea Moss Powder - Pharmaceutical Grade Bulk Supply

Product Code: EMN-ISMP-001

Latin Name:Chondrus crispus

Origin: Atlantic Coast (Ireland/Canada)

Processing Location: California, USA

Irish Sea Moss Powder

Product Overview

Whole Chandrus crispus from chilly Atlantic seas is used to make our Irish Sea Moss Powder. Mechanical cleaning, low-temperature drying, and micronization protect nutritional value.

Major Processing Steps:

1. Inspect raw materials for heavy metals and microorganisms.

2. Triple-wash system gets rid of sand and dirt.

3. Bioactivity is maintained by dehydration below 50°C.

4. Cryogenic milling offers 80-120 mesh homogeneity.

5. Packaging in drums with moisture barriers

This method reduces raw sea moss' irregularity while preserving its gelling and thickening carrageenan content.

Key Product Specifications

Parameter Specification
Latin Name Chondrus crispus
Appearance Fine white to light yellow powder
Plant Part Used Whole
Mesh Size 80-120
Moisture Content ≤12%
Package 25kgs/drum
MOQ 25kgs
Lead Time In stock, 2nd day pickup
Sample Free sample available

Certifications and Quality Standards

Certification Status
NSF GMP Certified
Kosher Certified
Halal Certified
ISO Certified
FSSC22000 Certified
Organic Certified
FDA Compliance Yes

Technical Advantages for Manufacturing

Consistent Particle Distribution

Equal liquid dispersion is achieved using 80-120 mesh. All batches have D90 < 180μm particle size analysis by laser diffraction.

Increases powder blend homogeneity and reduces beverage settling.

Minimum Moisture

Desiccant packing keeps moisture below 2%.

Irish Sea Moss Powder effectively prevents clumping and increases shelf life without preservatives.

Hydration Prediction

Absorbing 80-100ml water, 1g powder becomes stable gel.

Reduces batch-to-batch fluctuation and simplifies formula scaling.

Clear Label

One-ingredient product without solvents, carriers, or anti-caking and

Practicality: Meets food and supplement clean label regulations.

Applications and Uses

Quality Control Protocol

Every production batch undergoes:

Identity Testing

· Organoleptic evaluation (color, odor, taste)

· Microscopic identification

· DNA barcoding for species verification

Purity Testing

· Heavy Metals(ICP-MS method):

· Lead: < 2 ppm

· Arsenic: < 0.5 ppm

· Cadmium: < 0.5 ppm

· Mercury: < 0.1 ppm

· Microbiology:

· Total Plate Count: < 5,000 CFU/g

· Yeast/Mold: < 100 CFU/g

· E. coli: Negative/10g

· Salmonella: Negative/25g

Functional Testing

· Ash content (indicator of mineral content): 15-25%

· Acid-insoluble ash (sand/silica contamination): < 1%

· Gel strength testing (1.5% solution)

Documentation provided: COA, specification sheet, allergen statement, GMO declaration, BSE/TSE certificate.

Rigorous Quality Control Standards

Safety Testing Protocol

Test Parameter Specification Method
Lead <3ppm ICP-MS
Arsenic <1ppm ICP-MS
Cadmium <1ppm ICP-MS
Mercury <0.1ppm ICP-MS
Total Plate Count <5,000 CFU/g USP
Salmonella Negative AOAC
E. coli Negative AOAC
Yeast/Mold <100 CFU/g USP

Target Applications

Dietary Supplements

· Capsules and tablets (direct compression or wet granulation)

· Powder blends (smoothie mixes, meal replacements)

· Liquid supplements (suspensions, syrups)

Typical usage: 500-2,000 mg per serving

Food & Beverage

· Plant-based dairy alternatives (texture modifier)

· Protein bars and energy bites (binder)

· Soups and sauces (thickener)

Typical usage: 0.1-0.5% by weight

Cosmetics

· Face masks and body wraps (gel base)

· Hair conditioners (slip agent)

· Lotions and creams (emulsion stabilizer)

Typical usage: 1-3% in final formulation

R&D and Quality

Storehouse

FAQ

Q: How does powder differ from entire leaf?

A: Without soaking or combining, powder disperses immediately. Hydrating and manually processing whole leaf takes 12-24 hours.

Q: What is the gelling temperature?

A: Powder dissolves in cold water but thickens at 80-85°C and room temperature.

Q: Does it work with acidic formulations?

A: Below pH 4.5, carrageenan stability declines. Test matrix stability or use buffering agents.

Q: Can it replace synthetic thickeners?

A: Yes, numerous uses. Adjust to desired viscosity from 1:1. Our techies can help with conversion.

Q: What is the iodine content?

A: Usually 5-15 ppm, much below safety limits but sufficient for thyroid support medications (see local restrictions).

Ordering Information

Standard Order

· MOQ: 25kg (1 drum)

· Pricing: Contact for volume-based quotation

· Payment terms: Net 30 for qualified accounts

· Shipping: FOB from CA, NJ, TX, or IL warehouse

Sample Request

Free 100g sample available for qualified B2B buyers.

Request via:info@em-herb.com

Custom Requirements

We accommodate:

· Private labeling

· Custom packaging sizes

· Certificate modifications for specific markets

· Expedited shipping

Why Work With Earth Made Nutritions

The 4 U.S. warehouses assure regional availability and lower delivery costs.

Inventory management: Customer portal provides real-time stock view (after account creation).

Compliance support: Our staff handles GRAS affirmation, NDI alerts, and foreign export documents.

Technical service: First-order formulation consulting. Continuous product development assistance.

From harvest to delivery, full supply chain transparency. Request supplier audit reports.

Get Started

Do you have more questions about Irish Sea Moss Powder?

For samples or quotations: info@em-herb.com

Standard Disclaimer (DSHEA):
These statements have not been evaluated by the Food and Drug Administration.
This product is not intended to diagnose, treat, cure, or prevent any disease.
Sample Disclaimer
The samples provided are for evaluation and testing purposes only. They are not for commercial sale, human consumption, or medical use. Recipients must conduct their own testing to verify product suitability for their intended application.
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