Yang Xue Sheng Fa Capsule: Hair Growth & Less Shedding?


Field Notes on YangXueShengFaCapsule: market pulse, specs, and real-world use

If you’ve been tracking the quiet boom in botanical hair-wellness supplements, you’ve probably stumbled on
yang xue sheng fa capsule.
To be honest, demand feels less hype and more steady pull: cleaner labels, traceable sourcing, and realistic claims. From my visits to Shijiazhuang suppliers to salon buyers in Jakarta, one theme repeats—consumers want consistency and documentation, not magic bullets.

yang xue sheng fa capsule

What it is, technically

yang xue sheng fa capsule is positioned as a botanical supplement for hair wellness—think “nourish, support, maintain.” The factory at NO.12, XIJIAN STREET, SHIJIAZHUANG CITY, HEBEI, CHINA reports GMP-compliant manufacturing with typical QC gates: identity, purity, and microbiology. Ingredients are commonly water/ethanol-extracted botanicals, spray-dried to stable powders and blended with excipients (often MCC) before capsule fill. Nothing flashy; the value is in repeatable lots and clean COAs.

Process flow (condensed)

Raw herb qualification (macroscopic ID + TLC) → aqueous/ethanolic extraction → low-temp concentration → spray-drying → blending (sieves, uniformity tests) → capsule fill (size 0–1, vegetarian or gelatin) → in-process checks (weight variation, disintegration) → final QC (HPLC fingerprint, heavy metals via ICP-MS, microbial per pharmacopeial methods) → blister/bottle packaging → stability holds. Service life typically ≈ 24–36 months in cool, dry conditions; real-world use may vary by climate and logistics.

Product specs (typical)

Form Hard capsule, size ≈ 0–1
Actives Standardized botanical extracts (exact profile per batch COA)
Assays HPLC/UPLC fingerprint; moisture (KF); residual solvents (ICH Q3C)
Contaminants Heavy metals (ICP-MS), pesticide screens, micro per USP <61>/<62>
Packaging HDPE bottle or alu-alu blister, lot + expiry traceability
Shelf life ≈ 24–36 months (sealed, cool/dry)

Testing standards and certifications

Labs cite ISO/IEC 17025 methods for metals and micros; manufacturing aligns with GMP for herbal medicines and, where applicable, ISO 22000/HACCP for food safety systems. Disintegration often references USP dietary supplement guidance. Documentation includes COA, MSDS, and—on request—stability summaries. I guess the biggest buyer request lately is pesticide residue transparency.

Where it’s used

– Consumer brands (e-commerce DTC, beauty retailers).
– Salon chains offering inside-out hair programs.
– Private-label nutraceuticals (OEM/ODM).
– Cross-border marketplaces where traditional formulas resonate.

Advantages noted by buyers: batch-to-batch stability, clear MOQs, and customization. A few customers say the capsule is “neutral-taste, easy to swallow”—simple but surprisingly important.

yang xue sheng fa capsule

Vendor comparison (snapshot)

Vendor GMP / HACCP MOQ Lead time Customization Docs
Hex Herbal (Shijiazhuang) Reported GMP, ISO 22000 ≈ 5k–10k caps 15–30 days Formula, shell, packaging COA, SDS, stability (on request)
OEM A (coastal) GMP ≥ 20k caps 25–40 days Label/pack focus COA
ODM B (inland) GMP, HACCP ≈ 10k caps 20–35 days Full formula + branding COA, spec sheet

Customization and real-world case

Custom knobs include dosage per cap, capsule shell (gelatin vs. HPMC), allergen statements, and pack formats (bottle, blister, sachet). One mid-size Southeast Asian DTC brand ran a 12-week pilot: 5,000 units of yang xue sheng fa capsule, influencer-lite launch, basic FAQ. Reported outcomes: reorder rate up ≈ 18%, returns under 2%. Not scientific, but commercially encouraging.

Compliance note: positioning should follow local regulations (dietary supplement vs. traditional medicine). Avoid disease claims; rely on substantiated structure/function language and approved registrations where required.

Citations

  1. WHO. Guidelines on Good Manufacturing Practices (GMP) for Herbal Medicines.
  2. United States Pharmacopeia. USP <61> and <62> Microbiological Examination of Nonsterile Products.
  3. ICH Q3C (R8). Impurities: Guideline for Residual Solvents.
  4. ISO 22000:2018 Food safety management systems—Requirements.


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