Home › NDC Lookup › Ingredients › Chanvida Broad Spectrum Bb Cream › 84148-0027-01
Chanvida Broad Spectrum BB Cream .01 g/100g; .001 g/100g; .001 g/100g; .001 g/100g; 9.7 g/100g; .01 g/100g; .11 g/100g Cream, 50 g — NDC 84148-0027-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Chanvida Broad Spectrum BB Cream .01 g/100g; .001 g/100g; .001 g/100g; .001 g/100g; 9.7 g/100g; .01 g/100g; .11 g/100g Cream, 50 g — NDC 84148-027-01 (Billing 84148-0027-01)

by Guangzhou Ariel Biotech Co., Ltd. · 50 g in 1 BOTTLE

This is a package of 50 g of Chanvida Broad Spectrum BB Cream .01 g/100g; .001 g/100g; .001 g/100g; .001 g/100g; 9.7 g/100g; .01 g/100g; .11 g/100g Cream from Guangzhou Ariel Biotech Co., Ltd., marketed since Apr 2026 and currently FDA-listed. It is this product's only package size.

NDC 84148-0027-01
🏷️ FDA NDC (as labeled) 84148-027-01 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 Oct 1, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84148-027-01
Product NDC 84148-027
11-digit billing NDC 84148002701
UNII G2SH0XKK91, 38H206R00R, L4EL31FWIL, Y1DFQ308G8, SOI2LOH54Z, 2788Z9758H +4 more
Application # M020
SPL Set ID 4f8ade09-4f7a-80bd-e063-6394a90a0843
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Cell-mediated Immunity; Increased Histamine Release
Chemical class Allergens; Dietary Proteins; Plant Proteins
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-16
Route CUTANEOUS
Dosage form CREAM
Substance RETINOL; DIPEPTIDE DIAMINOBUTYROYL BENZYLAMIDE DIACETATE; ACETYL HEXAPEPTIDE-8; ACETYL TETRAPEPTIDE-5; ZINC OXIDE; GLYCYRRHIZA GLABRA (LICORICE) ROOT; SODIUM HYALURONATE; ALPHA-TOCOPHEROL ACETATE; 3-O-ETHYL ASCORBIC ACID; NIACINAMIDE
Why two NDCs? The FDA registers this code as 84148-027-01 — 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 → 84148-0027-01. 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?

Chanvida Broad Spectrum BB Cream is an over-the-counter cosmetic skin cream applied directly to the face and body. It contains vitamin C derivative (3-O-ethyl ascorbic acid), vitamin E acetate, retinol, and niacinamide, which are commonly used in skincare products for their antioxidant and skin-conditioning properties. The formula also includes peptides, licorice root extract, sodium hyaluronate (a humectant), and zinc oxide, ingredients typically found in products intended to moisturize, soothe, and protect the skin. This is an OTC monograph product regulated under FDA's standard rules for cosmetic and OTC drug combinations.

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 gPer 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
84148-0027-01 You're viewing this Main listing 50 g in 1 BOTTLE 2026-04-16 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Chanvida Broad Spectrum BB Cream .01 g/100g; .001 g/100g; .001 g/100g; .001 g/100g; 9.7 g/100g; .01 g/100g; .11 g/100gthis 84148-0027-01 Guangzhou 50 g — — 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
Apr 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.

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.

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 72VUP07IT5
    Alpha-arbutin is a plant-derived compound that acts as a skin-lightening agent and preservative in topical products. It helps stabilize formulations while providing cosmetic benefits in creams and lotions.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII XHK3U310BA
    Cyclohexasiloxane is a silicon-based liquid that acts as a solvent and conditioning agent in medicines. It helps dissolve or carry other ingredients and improves how the product spreads or feels on the skin.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII ANQ870JD20
    A synthetic chemical compound used as a UV filter in topical formulations. It protects the medicine or product from degradation caused by sunlight exposure during storage and use.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 4Y5P7MUD51
    A chemical compound that absorbs ultraviolet light. It is used in topical medicines and sunscreen products as a UV filter to help protect formulations from light degradation and to provide sun protection in the final product.
  • UNII 4X49Y0596W
    Ethylhexyl salicylate is a synthetic organic compound used as a UV filter and penetration enhancer in topical formulations. It helps protect the product and skin from ultraviolet light damage.
  • UNII XQN8R9SAK4
    A synthetic ultraviolet filter compound used in topical formulations to absorb and protect against harmful UV rays. It functions as an active sunscreen agent rather than a traditional inactive filler or binder.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • UNII 7QQ1EE6RCP
    A synthetic compound made from menthone and glycerin, used in medicines as a flavoring agent and fragrance ingredient. It provides a cooling or minty taste and aroma to make medications more pleasant to take.
  • UNII 5A68WGF6WM
    Octocrylene is a synthetic organic compound used in medicines as a UV filter and light-protective agent. It helps shield the active ingredients from degradation caused by sun exposure.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 46P231IQV8
    A synthetic emulsifier derived from glycerin and fatty acids. It helps blend oil and water-based ingredients together in cosmetic and pharmaceutical formulations to create stable, uniform products.
  • UNII 7F465U79Q1
    A clay mineral treated with a quaternary ammonium compound to make it water-soluble. Used as a thickener, suspending agent, and stabilizer to give products a smooth texture and prevent separation of ingredients.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII GW89575KF9
    Squalane is a lightweight oil derived from plant sources or synthesized. It acts as an emollient and lubricant in formulations, helping ingredients blend smoothly and improving product texture and spreadability.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII 8OC9U7TQZ0
    Tribehenin is a waxy, plant-derived substance that acts as a lubricant and glidant in tablets and capsules. It helps the medicine flow smoothly during manufacturing and prevents sticking during production and packaging.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.

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

The official label also states1,2-Hexanediol, Alpha-arbutin, Bht, Butylene Glycol, Cetyl Peg/ppg-10/1 Dimethicone, Ci 77491, Ci 77492,Ci 77499, Ci 77891, Cyclohexasiloxane, Cyclopentasiloxane, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dimethicone, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Ethylhexyl Triazone, Ethylhexylglycerin, Fragrance,Glycerin, Isohexadecane, Menthone Glycerin Acetal, Octocrylene, Phenoxyethanol, Polyglyceryl-3 Diisostearate, Quaternium-18 Bentonite, Silica, Sodium Chloride, Squalane, Talc, Titanium Dioxide, Tribehenin, Triethoxycaprylylsilane

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 Ariel Biotech Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84148
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio23 products on file
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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use Use only as directed. Avoid contact with eyes, eyelids, and mucous membranes.

⏱️ Dosage and Administration 59 words ▾

Directions 1. Apply as the final step of your morning skincare routine. 2. Dispense an adequate amount (approximately two finger-lengths) onto fingertips. 3. Apply evenly to the face, neck, and décolletage 15 minutes before sun exposure. 4. Gently pat into skin until fully absorbed. 5. Reapply at least every two hours, or immediately after swimming, sweating, or towel drying.

⚠️ Warnings 25 words ▾

Warnings For external use only. Sun Protection Message: This product provides sun protection. However, limiting sun exposure and wearing protective clothing (hats, sunglasses) is recommended.

📦 Storage and Handling 12 words ▾

Other information Store in a cool, dry place away from direct sunlight.

🧪 Active Ingredient 35 words ▾

Active Ingredient(s) Zinc Oxide 9.7% Niacinamide 2.5% 3-O-Ethy| Ascorbic Acid 1% Tocophery| Acetate 0.5% Sodium Hyaluronate 0.11% Glycyrrhiza Glabra(Licorice) Root Extract 0.01% Retinol 0.01% Dipeptide Diaminobutyroyl Benzylamide Diacetate 0.001% Acetyl Hexapeptide-8 0.001% Acetyl Tetrapeptide-5 0.001%

🧪 Inactive Ingredients 51 words ▾

Inactive ingredients 1,2-Hexanediol, Alpha-arbutin, Bht, Butylene Glycol, Cetyl Peg/ppg-10/1 Dimethicone, Ci 77491, Ci 77492,Ci 77499, Ci 77891, Cyclohexasiloxane, Cyclopentasiloxane, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Dimethicone, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Ethylhexyl Triazone, Ethylhexylglycerin, Fragrance,Glycerin, Isohexadecane, Menthone Glycerin Acetal, Octocrylene, Phenoxyethanol, Polyglyceryl-3 Diisostearate, Quaternium-18 Bentonite, Silica, Sodium Chloride, Squalane, Talc, Titanium Dioxide, Tribehenin, Triethoxycaprylylsilane

🎯 Purpose 12 words ▾

Purpose Sunscreen Brightening/anti-acne Brightening Hydration Hydration Soothing nti-aging/ Anti-acne Anti-aging Anti-aging Anti-aging

📄 Do Not Use 10 words ▾

Do not use Do not Use if pregnant or nursing.

📄 When Using This Product 24 words ▾

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water. Discontinue use if any irritation or adverse reaction occurs.

📄 Stop Use and Ask a Doctor If 9 words ▾

Discontinue use if any irritation or adverse reaction occurs.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Package Label / Principal Display Panel 7 words ▾

Package Label - Principal Display Panel undefined

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

About this NDC listing & data coverage

Over-the-counter (OTC) product
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 "Otc Monograph Drug". 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 Ariel Biotech Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Ariel Biotech 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.
← 84148-0026-01 · Guangzhou 84148-0028-01 · Guangzhou →
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.