Supplement Label Index
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Berberine

Of 479 on-market berberine products in the January 2026 DSLD dump, the median declared dose is 500 mg, and 93.1% list Berberine HCl (Hydrochloride) as the primary form.

479
on-market products
500 mg
median dose
below RDA
above UL
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Form share

Of 462 products with an identifiable primary form, here is the share held by each form of Berberine on the market today.

Berberine HCl (Hydrochloride) 93.1% Berberis aristata extract (source-plant labeling) 6.7% Berberine Sulfate 0.2%
FormQuality tiernShare
Berberine HCl (Hydrochloride) Tier 1 430 93.1%
Berberis aristata extract (source-plant labeling) Tier 2 31 6.7%
Berberine Sulfate Unrated 1 0.2%

Form share over time

Entry-year breakdown of the top forms, 2012–2025.

Berberine HCl (Hydrochloride)Berberis aristata extract (source-plant labeling)Berberine Sulfate20122013201420152016201720182019202020212022202320242025

Dose distribution

Deciles of declared dose per serving (mg), among 361 products with a disclosed amount.

p10p20p30p40p50p60p70p80p90Fairy-dust
  • 10.0% of products fall below the fairy-dust threshold (60 mg, 20% of the studied low dose).
  • 21.3% of products don't disclose an amount because Berberine is declared inside a proprietary blend.

By dosage form

Capsule 414 Powder 21 Tablet or Pill 18 Liquid 14 Other (e.g. tea bag) 6 Softgel Capsule 6

By target group

Adult (18 - 50 Years) 467 Gluten Free 242 Dairy Free 177 Women (not pregnant or lactating) 146 Vegetarian 139 Vegan 100 Sugar Free 69 Kosher 11

Top brands

Forms explained

Berberine HCl (Hydrochloride) Tier 1

The form used in the overwhelming majority of clinical trials, including the metformin-comparison trial and most diabetes/lipid meta-analysis literature -- despite known poor intrinsic oral bioavailability (~5% or less), it has the deepest outcome-level human evidence.

Source: Yin J et al. 2008, Metabolism 57(5):712-7, PMID 18442638

Berberine Sulfate Unrated

A 2003 patent claims improved water solubility/absorption vs the chloride salt, but no independent human clinical outcome trial specific to the sulfate salt was located.

Source: uncertain -- needs review (patent claim only, WO2003090749A1)

Berberis aristata extract (source-plant labeling) Tier 2

Typically the same berberine-HCl active compound sourced/standardized from whole-plant extract, used in several of the same clinical trials as "berberine," but whole-extract products can vary in standardized berberine content and carry co-extracted alkaloids.

Source: e.g. HIMABERB (Berberis aristata-derived) prediabetes RCT, PMC10483788

Reference values

  • RDA (adult): not established — Plant alkaloid, not an essential nutrient; no DRI exists.
  • Tolerable Upper Intake Level (adult): not established — Not established. Clinical trials up to ~1500mg/day for 3-12 months report GI side effects (diarrhea, constipation, abdominal pain) as the main dose-limiting issue.
  • Studied clinical dose range: 300–1500 mg
  • Yin J et al. 2008, Metabolism 57(5):712-7, PMID 18442638 -- RCT (n=36) newly-diagnosed type 2 diabetics, 500mg TID (1500mg/day) berberine vs metformin 500mg TID x3 months; comparable glucose-lowering (HbA1c 9.5%->7.5%, fasting glucose 10.6->6.9 mmol/L, both P<0.01) plus a triglyceride reduction.
  • Note: category is 'other' rather than 'amino' -- berberine is a plant isoquinoline alkaloid, not an amino acid.
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