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SEVICH CHEBE HAIR BIOTIN 400 mg/mL; 200 mg/mL; 2 mg/mL Oil, 30 mL — NDC 87655-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

SEVICH CHEBE HAIR BIOTIN 400 mg/mL; 200 mg/mL; 2 mg/mL Oil, 30 mL — NDC 87655-001-01 (Billing 87655-0001-01)

by Guangzhou Sanwich Biology Technology Co., Ltd · 30 mL in 1 BOTTLE

This is a package of 30 mL of SEVICH CHEBE HAIR BIOTIN 400 mg/mL; 200 mg/mL; 2 mg/mL Oil from Guangzhou Sanwich Biology Technology Co., Ltd, marketed since Jul 2026 and currently FDA-listed. It is this product's only package size.

NDC 87655-0001-01
🏷️ FDA NDC (as labeled) 87655-001-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 87655-001-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87655 labeler · 001 product · 01 package
Package marketed since
Jul 3, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8765500101 0
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87655-001-01
Product NDC 87655-001
11-digit billing NDC 87655000101
UNII 515610SU8C, 9JS8DS42SV, 6SO6U10H04
SPL Set ID 55b0b7f8-5ac1-f325-e063-6294a90a0b16
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-03
Route TOPICAL
Dosage form OIL
Substance MACADAMIA TERNIFOLIA SEED OIL; CALENDULA OFFICINALIS SEED OIL; BIOTIN
Why two NDCs? The FDA registers this code as 87655-001-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 87655-0001-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

Sevich Chebe Hair Biotin Oil is a topical oil product that combines biotin, a B vitamin commonly included in hair care products to support hair structure, with calendula and macadamia seed oils, which are plant-derived moisturizing and conditioning agents typically used in cosmetic hair treatments. This product is marketed as an unapproved drug and has not received FDA approval. The oil is applied directly to the hair and scalp.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
87655-0001-01 You're viewing this Main listing 30 mL in 1 BOTTLE 2026-07-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Sevich Chebe Hair 400 mg/mL; 200 mg/mL; 2 mg/mLthis 87655-0001-01 Guangzhou 30 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color brown
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • 0.01 mL / 1 mL UNII H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • 0.02 mL / 1 mL UNII 2JYC99Q0WZ
    A plant extract from Artemisia argyi, commonly known as mugwort. It may be used as a flavoring agent, fragrance, or traditional botanical ingredient in some formulations.
  • 0.08 mL / 1 mL UNII U37N0S910T
    A natural oil extracted from camellia seeds, used as an emollient and conditioning agent. It helps soften the product texture and improve skin feel in topical formulations.
  • 0.05 mL / 1 mL UNII A4WO0626T5
    A natural aromatic oil extracted from cinnamon bark, used as a flavoring agent to improve taste and add spice notes to medicines.
  • 0.01 mL / 1 mL UNII 578389D6D0
    Clove oil is an essential oil derived from clove plant buds. It's used in medicines as a flavoring agent and for its mild preservative properties to help maintain product stability.
  • 0.1 mL / 1 mL UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • 0.001 mL / 1 mL UNII R66Z4YW3X0
    A plant-derived or synthetic aromatic ingredient that adds pleasant smell to the medicine. Fragrances mask unpleasant tastes or odors in oral medications to make them easier to take.
  • 0.017 mL / 1 mL UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • 0.01 mL / 1 mL UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • 0.05 mL / 1 mL UNII 1L29G6428X
    A plant extract from bitter cherry fruit used as a natural flavoring agent and colorant in medicines. It adds taste and visual appeal to the product while remaining inactive in terms of therapeutic effect.
  • 0.05 mL / 1 mL UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.

11 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive Ingredients: Cocos Nucifera (Coconut) Oil, Cinnamomum Cassia Oil, Fragrance Floral, Artemisia Argyi Leaf, Alpha-Tocopherol, Camellia Japonica Seed Oil, Lavender Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Clove Oil, Prunus Cerasus (Bitter Cherry) Fruit Extract.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerGuangzhou Sanwich Biology Technology Co., Ltd
Labeler code87655
First marketedJul 2026
Product typeHuman Otc Drug
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

INDICATIONS & USAGE SECTION Uses: Helps moisturize dry scalp and hair. Helps improve the appearance of dry, brittle and frizzy hair. Helps reduce the appearance of hair breakage caused by dryness.

⏱️ Dosage and Administration 17 words ▾

Directions Directions: Apply a proper amount to scalp and hair. Massage gently until absorbed. Use as needed.

⚠️ Warnings 33 words ▾

Warnings Warnings: For external use only. Avoid contact with eyes and sensitive skin areas. Do not use on broken or irritated skin. Discontinue use if irritation occurs. Keep out of reach of children.

🧪 Active Ingredient 16 words ▾

Active Ingredients Active Ingredients: Macadamia Ternifolia Seed Oil 40% Calendula Officinalis Seed Oil 20% Biotin 0.2%

🧪 Inactive Ingredients 42 words ▾

Inactive Ingredients Inactive Ingredients: Cocos Nucifera (Coconut) Oil, Cinnamomum Cassia Oil, Fragrance Floral, Artemisia Argyi Leaf, Alpha-Tocopherol, Camellia Japonica Seed Oil, Lavender Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Clove Oil, Prunus Cerasus (Bitter Cherry) Fruit Extract.

🎯 Purpose 6 words ▾

Purpose Purpose: Hair and scalp conditioning.

📋 Description 15 words ▾

Other Information Other Information: Store in a cool, dry and ventilated place. Avoid direct sunlight.

📄 Keep Out of Reach of Children 12 words ▾

Keep Out of Reach of Children Keep out of reach of children.

📄 Package Label / Principal Display Panel 33 words ▾

Principal Display Panel SEVICH CHEBE HAIR OIL NDC: 87655-001-01 Net Contents: 30 mL / 1.0 fl. oz. For external use only. Moisturize, repair and protect dry scalp and hair. SEVICH CHEBE HAIR OIL

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for SEVICH CHEBE HAIR (this brand).

Top reported reactions

Fatigue3,177
Nausea2,352
Headache2,249
Alopecia2,245
Diarrhoea1,983
Pain1,777
Dizziness1,652

Age at onset

Neonate20
Infant21
Child16
Adolescent37
Adult3,294
Elderly2,986

Reporter sex

31,021 reports
Male · 10%
Female · 90%
Unknown · 0%

Serious outcomes

Hospitalization5,784
Disabling1,037
Death966
Life-threatening569
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,722 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Drug Other". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Guangzhou Sanwich Biology Technology Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Sanwich Biology Technology Co., Ltd is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 87654-0001-01 · MIYOSHI 87656-0964-04 · Triplicare →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.