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Veakson Beef Tallow Sunscreen Zinc Oxide,Phenylbenzimidazole Sulfonic Acid 20 g/100g; 1 g/100g Cream, 60 g — NDC 83566-0563-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Veakson Beef Tallow Sunscreen Zinc Oxide,Phenylbenzimidazole Sulfonic Acid 20 g/100g; 1 g/100g Cream, 60 g — NDC 83566-563-01 (Billing 83566-0563-01)

by Guangdong Aimu Biological Technology Co., Ltd · 60 g in 1 BOTTLE, GLASS

This is a package of 60 g of Veakson Beef Tallow Sunscreen Zinc Oxide,Phenylbenzimidazole Sulfonic Acid 20 g/100g; 1 g/100g Cream from Guangdong Aimu Biological Technology Co., Ltd, marketed since Jan 2026 and currently FDA-listed. It is this product's only package size.

NDC 83566-0563-01
🏷️ FDA NDC (as labeled) 83566-563-01 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 83566-563-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83566 labeler · 563 product · 01 package
Package marketed since
Jan 4, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
6941858901856
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83566-563-01
Product NDC 83566-563
11-digit billing NDC 83566056301
UNII SOI2LOH54Z, 9YQ9DI1W42
UPC 6941858901856
Application # M020
SPL Set ID 473c241a-1258-1680-e063-6394a90a7d98
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-01-04
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; PHENYLBENZIMIDAZOLE SULFONIC ACID
Why two NDCs? The FDA registers this code as 83566-563-01 — 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 → 83566-0563-01. 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?

Veakson Beef Tallow Sunscreen is a topical cream classified as an over-the-counter monograph drug. It contains two active ingredients that function as ultraviolet (UV) filters: zinc oxide, a mineral sunscreen agent that reflects UV rays, and phenylbenzimidazole sulfonic acid, a chemical sunscreen agent that absorbs UV radiation. These ingredients are commonly used together in sunscreen products to help protect skin from sun exposure when applied to exposed skin surfaces.

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
83566-0563-01 You're viewing this Main listing 60 g in 1 BOTTLE, GLASS 2026-01-04 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Veakson Beef Tallow Sunscreen 20 g/100g; 1 g/100gthis 83566-0563-01 Guangdong 60 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
Jan 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 98HPY76U4W
    Beef tallow is a fat rendered from cattle tissue. It's used in medicines as a lubricant and binder to help tablets form properly and slide through machinery during manufacturing.
  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 7H8VAM7778
    A synthetic compound derived from cetyl alcohol and ethylene oxide. It acts as an emulsifier and surfactant in medicines, helping blend water and oil-based ingredients together into a stable, uniform product.
  • 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 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 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • 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 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 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • 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 6DRV3D37XS
    A plant extract from Chinese lizard's tail (Saururus chinensis), used in traditional herbal preparations. It serves as an active botanical ingredient that may provide therapeutic properties, though its specific formulation role in this product depends on the medicine's intended use.
  • 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 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.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 7S7TV2F4XC
    A plant extract from Stephania tetrandra, a vine used traditionally in herbal preparations. In medications, it may serve as an active botanical ingredient or provide binding and consistency properties to the formulation.
  • UNII 9DE5YCO0RU
    A plant extract from dandelion root traditionally used in herbal preparations. In medications, it may serve as a flavor enhancer, natural colorant, or bitter component that supports formulation taste and appearance.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWATER 31.76% ETHYLHEXYL SALICYLATE 5% ADEPS BOVIS 5% C12-15 ALKYL BENZOATE 4% CETEARYL ALCOHOL 3.5% SQUALANE 3% DIMETHICONE 3% GLYCERYL STEARATE 3% ISONONYL ISONONANOATE 3% BUTYROSPERMUM PARKII (SHEA) BUTTER 3% SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL 3% OLEA EUROPAEA (OLIVE) FRUIT OIL 2% BEESWAX 2% SILICA 2% TOCOPHERYL ACETATE 1% C20-24 ALKYL DIMETHICONE 1% XANTHAN GUM 0.6% CETETH-2 0.5% LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE 0.5% SAURURUS CHINENSIS LEAF/ROOT EXTRACT 0.5% TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT 0.5% STEPHANIA TETRANDRA EXTRACT 0.5% PHENOXYETHANOL 0.45% LECITHIN 0.1% ETHYLHEXYLGLYCERIN 0.05% DISODIUM EDTA 0.02% CI 77492 0.02%

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

LabelerGuangdong Aimu Biological Technology Co., Ltd
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code83566
First marketedJan 2026
Product typeHuman Otc Drug
Portfolio39 products on file

More NDCs from Guangdong Aimu Biological Technology Co., Ltd labeler code 83566

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 📄 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 60 words ▾

Uses Ensure skin is clean and dry before use. Shake well before use. Apply generously 15 minutes before sun exposure; Reapply: every 2 hours or immediately after swimming, sweating, or towel drying. Minimize sun exposure, especially between 10 AM and 2 PM, and wear long-sleeved clothing, long pants, a hat, and sunglasses; For children under 6 months: Consult a doctor.

⏱️ Dosage and Administration 10 words ▾

Dosage & administration Apply generously 15 minutes before sun exposure.

⚠️ Warnings 38 words ▾

Warnings For external use only. SkinCancer/SkinAging Alert :Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, notskin cancer or early skin aging.

🧪 Active Ingredient 9 words ▾

Active Ingredients ZINC OXIDE 20% PHENYLBENZIMIDAZOLE SULFONIC ACID 1%

🧪 Inactive Ingredients 92 words ▾

Inactive ingredients WATER 31.76% ETHYLHEXYL SALICYLATE 5% ADEPS BOVIS 5% C12-15 ALKYL BENZOATE 4% CETEARYL ALCOHOL 3.5% SQUALANE 3% DIMETHICONE 3% GLYCERYL STEARATE 3% ISONONYL ISONONANOATE 3% BUTYROSPERMUM PARKII (SHEA) BUTTER 3% SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL 3% OLEA EUROPAEA (OLIVE) FRUIT OIL 2% BEESWAX 2% SILICA 2% TOCOPHERYL ACETATE 1% C20-24 ALKYL DIMETHICONE 1% XANTHAN GUM 0.6% CETETH-2 0.5% LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE 0.5% SAURURUS CHINENSIS LEAF/ROOT EXTRACT 0.5% TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT 0.5% STEPHANIA TETRANDRA EXTRACT 0.5% PHENOXYETHANOL 0.45% LECITHIN 0.1% ETHYLHEXYLGLYCERIN 0.05% DISODIUM EDTA 0.02% CI 77492 0.02%

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 11 words ▾

Do Not Use Do not use on damaged or broken skin.

📄 When Using This Product 13 words ▾

When Using Avoid contact with eyes. If contact occurs, rinse immediately with water.

📄 Stop Use and Ask a Doctor If 15 words ▾

Stop Use If a rash develops or the product is swallowed, seek medical assistance immediately

📄 Keep Out of Reach of Children 25 words ▾

Keep Out Of Reach Of Children Keep out of reach of children. If a rash develops or the product is swallowed, seek medical assistance immediately.

📄 Package Label / Principal Display Panel 4 words ▾

PRINCIPAL DISPLAY PANEL Label.

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 Guangdong Aimu Biological Technology Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangdong Aimu Biological 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.
← 83566-0562-01 · Guangdong 83566-0564-01 · Guangdong →
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.