이 제품에 대해 글로벌 공급망 인텔리전스 네트워크에 수출업체 1,198개와 수입업체 1,395개가 색인되어 있습니다.
2,052건의 공급업체 연계 거래가 상위 20개 국가에 걸쳐 요약되어 있습니다.
현재 프리미엄 공급업체 0개와 카탈로그 항목 0개가 등록되어 있습니다.
도매 샘플 항목: 0건; 산지가 샘플 항목: 0건.
페이지 데이터 최종 업데이트일: 2026-05-16.
비타민 D 보충제에 대한 글로벌 공급업체 거래, 수출 활동 및 가격 벤치마크
상위 20개 국가에 걸친 공급업체 연계 거래 2,052건을 분석하고, 월간 단가 벤치마크로 비타민 D 보충제의 수출 경쟁력과 소싱 리스크를 추적하세요.
비타민 D 보충제 국가별 공급업체 거래 및 수출 모멘텀 전년 대비 변화
비타민 D 보충제의 긍정적/부정적 전년 대비 변화를 비교해 성장하는 공급 시장과 약화되는 수출 경로를 식별하세요.
비타민 D 보충제의 YoY 변동 상위 국가는 영국 (+381.6%), 코스타리카 (+237.3%), 아랍에미리트 (+89.1%)입니다.
비타민 D 보충제 국가별 공급업체 거래 및 단가 요약
2025-06 기준으로 비타민 D 보충제 국가별 거래 건수와 월간 단가/물량을 비교해 공급업체 및 수출 시장 우선순위를 정하세요.
2025-11 기준, 노출 가능한 비타민 D 보충제 거래 단가가 있는 국가는 과테말라 (305.22 USD / kg), 독일 (196.81 USD / kg), 싱가포르 (176.66 USD / kg), 아랍에미리트 (151.36 USD / kg), 콜롬비아 (122.95 USD / kg), 외 13개국입니다.
Industry PositionFinished Dietary Supplement (Nutraceutical)
Market
Vitamin D supplements are globally traded consumer health products formulated primarily with vitamin D3 (cholecalciferol) or vitamin D2 (ergocalciferol) to support dietary intake. Demand is closely linked to public health guidance on vitamin D intake, seasonal/latitude-related sun exposure patterns, and clinical deficiency management, with widespread retail and cross-border e-commerce distribution. Market access is strongly shaped by jurisdiction-specific rules on permitted vitamin sources, maximum levels, and labeling/claims, with Codex providing international guidance for vitamin and mineral food supplements. Supply chains commonly involve an upstream vitamin ingredient market (vitamin D forms and premixes) feeding into contract manufacturing for finished dose forms, making quality control and label-claim accuracy central to trade credibility.
Market GrowthNot Mentioned
Specification
Major VarietiesVitamin D3 (cholecalciferol), Vitamin D2 (ergocalciferol)
Physical Attributes
Fat-soluble vitamin used in low-dose, high-potency formulations where small dosing errors can materially change intake
Compositional Metrics
Label declarations commonly expressed in micrograms (mcg) and/or International Units (IU) per serving
Potency (label-claim) verification and content uniformity are key quality-control expectations for finished dose forms
Grades
Finished products sold as regulated food supplements/dietary supplements in dose form (e.g., capsules, tablets, measured-dose liquids)
Packaging
Dose-form retail packs (e.g., bottles or blister packs) with declared vitamin D amount per serving and recommended daily intake guidance
ProcessingVitamin D2 is manufactured via UV irradiation of ergosterol from yeast; vitamin D3 is typically produced using 7-dehydrocholesterol from lanolin (sheep wool), with animal-free D3 alternatives sourced from lichen also available
Supply Chain
Value Chain
Vitamin D ingredient sourcing (D2 or D3) -> incoming material identity/potency checks -> premix/blending with excipients or carrier oils -> encapsulation/tableting/softgel filling -> packaging & labeling -> distribution via retail and e-commerce
Demand Drivers
Bone health positioning via vitamin D’s role in calcium absorption and maintaining serum calcium and phosphate levels
Use in deficiency prevention/management and in populations at risk of inadequate vitamin D status (as defined by health authorities)
Risks
Product Quality And Potency Control HighManufacturing or formulation failures can lead to vitamin D levels far above the label claim, creating acute consumer safety risk (e.g., hypercalcaemia/hypercalciuria) and triggering rapid recalls/withdrawals and import holds. Official food-safety alerts have occurred for supplements withdrawn due to excessive vitamin D content.Apply dietary-supplement cGMP with robust batch-release controls (identity, potency, and content-uniformity testing), supplier qualification for vitamin D inputs, and post-market complaint/traceability procedures for rapid withdrawal.
Regulatory Compliance MediumRules differ widely by jurisdiction for food supplements (permitted vitamin sources, maximum levels, labeling format, and allowable claims), increasing the risk of border rejections or mandatory relabeling when products are sold internationally.Maintain market-by-market regulatory specifications (allowed forms, maximum levels, claims wording) and align labels with Codex guidance plus local requirements before export.
Supply Chain Integrity MediumIngredient-origin and process differences (D2 vs D3; lanolin-derived vs lichen-derived D3) can create mislabeling risk for vegan/animal-origin claims and can affect buyer acceptance and compliance expectations.Use documented traceability for vitamin D inputs (form, source, and processing) and verify origin/claim statements through supplier audits and analytical testing where feasible.
Consumer Misuse And Overconsumption MediumHigh-dose vitamin D supplementation can cause toxicity and clinically significant hypercalcaemia, particularly when consumers combine multiple fortified foods/supplements or use high-dose products without medical oversight.Provide clear dose directions and warnings on labels, discourage stacking with other high-dose products, and implement responsible marketing that avoids encouraging unsupervised megadosing.
Sustainability
Animal-derived sourcing risk and claim sensitivity: vitamin D3 is typically produced from lanolin (sheep wool), while animal-free D3 (lichen) exists; origin traceability affects vegan/animal-origin claims and procurement policies
Labor & Social
Consumer protection and fair marketing risk: misleading claims and inaccurate labels are a recurring enforcement focus for supplements, especially in cross-border e-commerce
Labeling discipline expectations: Codex guidance emphasizes clear product identity, nutrient amounts, and intake directions for vitamin/mineral supplements to reduce consumer harm
FAQ
What is the difference between vitamin D2 and vitamin D3 in supplements?NIH’s Office of Dietary Supplements explains that vitamin D in supplements is mainly found as vitamin D2 (ergocalciferol) or vitamin D3 (cholecalciferol). Both can raise blood 25(OH)D levels, but NIH notes research showing D3 often increases and maintains 25(OH)D levels more than D2, and the two forms differ in how they are made and sourced (e.g., D2 from UV-treated yeast ergosterol; D3 typically from lanolin, with lichen-based D3 also available).
Why is incorrect vitamin D potency in supplements a serious risk?Vitamin D is potent, and excessive intake can lead to toxicity, including clinically significant hypercalcaemia/hypercalciuria; EFSA’s upper intake level work and medical references describe these adverse effects as key toxicity endpoints. Real-world enforcement actions have occurred, such as official food-safety alerts where supplements were withdrawn due to excessively high vitamin D content compared with what consumers would expect from labeling.
What global standards or rules shape vitamin D supplement labeling and compliance?Codex Alimentarius provides international guidance for vitamin and mineral food supplements (CAC/GL 55-2005), including expectations on product identity, declaring nutrient amounts, and directions for use. In practice, exporters also need to comply with jurisdiction-specific supplement frameworks (e.g., EU food supplement rules and national cGMP and labeling requirements such as those referenced by FDA for dietary supplements).