브라질 D-비오틴 원료 가격 및 무역 — 마켓 오버뷰 2026

상위 제품

비오틴

HS 코드

293629

최종 업데이트

2026-08-23

서치 및 소싱 팀을 위한 핵심 요약

수출 파트너 국가 5개와 수입 파트너 국가 5개가 랭킹되어 있습니다.
이 페이지 데이터셋의 최신 기준 연도는 2024입니다.
페이지 데이터 최종 업데이트일: 2026-08-23.

브라질 내 D-비오틴 원료 수출 공급업체 인텔리전스, 가격 추이 및 무역 흐름

Supply Chain Intelligence 기업 프로필 및 분석으로 브라질의 D-비오틴 원료 수출업체 커버리지, 파트너 품질, 경로 우선순위를 검증하세요.

브라질 내 D-비오틴 원료의 연간 수출 금액, 물량 및 공급업체 시장 규모 (HS 코드 293629)

브라질의 D-비오틴 원료 수출 물량/금액 3년치를 분석해 공급 측 시장 성장, 계절성, 무역 변동성을 평가하세요.

연도	물량	금액
2024	72,297,834	478,325,258 USD
2023	67,290,051	457,571,154 USD
2022	72,039,184	435,597,831 USD

브라질에서 수출되는 D-비오틴 원료의 주요 수출 대상 시장 (HS 코드 293629) 2024

2024년 기준, 브라질발 D-비오틴 원료 수출의 상위 목적지국 5개 전반에서 수출 물량과 금액을 비교하세요.

순위	국가	물량	금액
1	볼리비아	5,887,139	90,412,773 USD
2	미국	10,208,480.718	58,817,682 USD
3	베네수엘라	3,627,296	47,737,546 USD
4	파라과이	8,074,331	46,663,096 USD
5	콜롬비아	4,625,963	32,729,977 USD

소싱 진단

브라질산 D-비오틴 원료, 우리도 들여올 수 있을까요?

필요한 스펙과 물량만 알려주세요. 실제로 소싱이 되는지, 어떤 원산지와 공급사가 맞는지 무료로 짚어드려요.

브라질의 D-비오틴 원료 수입 바이어 인텔리전스 및 가격 시그널: 바이어, 수요, 거래 파트너

수출업체와 수입업체는 Supply Chain Intelligence 기업 프로필 및 분석으로 브라질의 D-비오틴 원료 구매 수요, 파트너 밀도, 다운스트림 채널을 분석할 수 있습니다.

브라질 내 D-비오틴 원료의 연간 수입 금액, 물량 및 수요 규모 (HS 코드 293629)

브라질의 D-비오틴 원료 수입 물량/금액 3년치를 추적해 수요 성장과 시장 모멘텀을 평가하세요.

연도	물량	금액
2024	50,938,775	427,922,959 USD
2023	47,645,038	358,615,307 USD
2022	45,929,274	306,008,846 USD

브라질에 D-비오틴 원료를 공급하는 주요 원산지 공급국 (HS 코드 293629) 2024

2024년 기준, 브라질로 D-비오틴 원료를 공급하는 상위 원산 공급국 5개 전반의 수입 물량과 금액을 비교하세요.

순위	국가	물량	금액
1	우루과이	3,205,775	86,742,579 USD
2	네덜란드	17,299,682	75,357,356 USD
3	미국	1,968,823.238	33,839,642 USD
4	중국	4,531,282.452	27,203,855 USD
5	아르헨티나	3,091,315	23,053,529 USD

수출 진단

우리 D-비오틴 원료, 이 브라질 바이어들에게 팔 수 있을까요?

만드시는 제품만 알려주시면 됩니다. 지금 수출할 준비가 됐는지, 어느 시장이 맞는지 무료로 봐드려요.

가격 데이터

가려진 브라질 D-비오틴 원료 가격, 열어볼까요?

전체 가격 히스토리와 경쟁사 벤치마크를 열어드립니다. 어떤 숫자가 필요하신지만 말씀해 주시면 함께 살펴봐 드려요.

Classification

Product TypeProcessed Food

Product FormOral dietary supplement (capsules/tablets/softgels/powder)

Industry PositionFinished Dietary Supplement Product

Market

In Brazil, biotin supplements are regulated as “suplementos alimentares” under ANVISA’s food framework, with composition, safety, and labeling requirements anchored in RDC 243/2018 and the complementary constituent/limits/claims lists in IN 28/2018. Biotin (D-biotin) is included in the authorized constituent lists, and authorized claim wording exists (e.g., metabolism support and maintenance of hair and skin) when the product meets the applicable composition conditions and limits. Market access risk is driven less by agronomic seasonality and more by regulatory compliance (constituent eligibility, dosage limits by population group, and strict claim/label controls). Imports and domestically manufactured/packed products both need to align with ANVISA’s sanitary requirements and, for import operations, the applicable government trade licensing/document workflows (e.g., LI/LPCO models in the Portal Único Siscomex context for food imports).

Market RoleDomestic consumer market with both imports and local manufacturing/packing

Domestic RoleConsumer-packaged supplement positioned around ANVISA-authorized biotin functions/claims (within the authorized wording and compositional conditions)

Specification

Physical Attributes

Products are presented in oral ‘pharmaceutical forms’ (e.g., capsules/tablets), consistent with ANVISA’s definition of suplemento alimentar and the required product designation format.

Compositional Metrics

The daily recommended intake on label must comply with the minimum and maximum limits defined in the applicable annexes of IN 28/2018 for the indicated population group(s), as required by RDC 243/2018.

Packaging

Portuguese labeling is central to acceptance: the product must be designated as “Suplemento Alimentar” plus its dosage form, and the label must include required warnings such as “Este produto não é um medicamento”, “Não exceder a recomendação diária de consumo indicada na embalagem”, and “Mantenha fora do alcance de crianças”, per RDC 243/2018.

Supply Chain

Value Chain

Active ingredient (biotin) sourcing and qualification → receipt and identity/purity checks against accepted references → blending with permitted excipients → encapsulation/tableting → packaging and label control → finished-product release (documentation retained for authority review) → distribution through regulated retail channels and/or import clearance flow when imported

Temperature

While biotin solid-dose supplements are typically less cold-chain dependent than fresh foods, stability through shelf-life must be ensured via stability studies and appropriate conservation instructions, as required by RDC 243/2018.

Shelf Life

Shelf-life claims must be supported by stability studies and quality controls, with documentation retained for competent authority consultation, per RDC 243/2018.

Freight IntensityLow

Transport ModeMultimodal

Risks

Regulatory Compliance HighNon-compliance with ANVISA’s supplement framework (RDC 243/2018 + IN 28/2018 lists/limits/authorized claims) can result in import delay, refusal, enforcement action, or market withdrawal—especially where biotin dosage, population-group limits, or claim wording/conditions do not match the authorized rules.Pre-validate formulation, daily intake, and all biotin-related label claims against RDC 243/2018 and the current IN list(s); keep a complete compliance dossier ready for authority review (specifications, stability rationale, labeling rationale).

Food Safety MediumDietary supplements face elevated scrutiny for contamination/adulteration risk; RDC 243/2018 explicitly disallows doping-listed and controlled substances in supplement composition, creating a high-impact compliance failure mode if suppliers are not tightly qualified.Implement supplier qualification and batch testing (identity, purity, contaminants) and require robust CoA and change-control; apply risk-based screening for prohibited substances where relevant.

Documentation Gap MediumBrazil’s import workflow for foods under sanitary intervention can involve LI/LPCO models and protocol steps that change over time; misaligned filings, fee-payment linkage issues, or incomplete submissions can create clearance delays and storage-cost escalation.Use an experienced customs broker familiar with ANVISA food-import LPCO requirements; track current Siscomex/ANVISA notices on LPCO model usage and fee-payment integration; reconcile product classification and dossier completeness before shipment.

FAQ

Can a biotin supplement in Brazil claim benefits for hair and skin?Yes—ANVISA’s IN 28/2018 includes authorized biotin-related claim wording (including maintenance of hair and skin), but the claim is conditional on meeting the rule’s compositional requirements and staying within the applicable minimum and maximum limits for the labeled daily intake.

What label warnings are mandatory for supplements in Brazil?RDC 243/2018 requires that supplements be designated as “Suplemento Alimentar” plus the dosage form and include mandatory warnings such as “Este produto não é um medicamento”, “Não exceder a recomendação diária de consumo indicada na embalagem”, and “Mantenha fora do alcance de crianças”.

Are doping substances allowed in Brazilian dietary supplements?No. RDC 243/2018 prohibits substances considered doping by WADA and substances subject to special control rules (as referenced by the regulation), so products and raw materials must be qualified to avoid prohibited-substance risk.