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Le Mieux Naked Glow Bronzer SPF 50 Sunscreen 8 g/100g; 4 g/100g; 3 g/100g; 5 g/100g Gel — NDC 81208-0206-02 package photo

Le Mieux Naked Glow Bronzer SPF 50 Sunscreen 8 g/100g; 4 g/100g; 3 g/100g; 5 g/100g Gel

by YB CHEMIA LLC · 1 TUBE in 1 CARTON (81208-206-02) / 50 g in 1 TUBE
NDC 81208-0206-02
🏷️ FDA NDC (as labeled) 81208-206-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 81208-206-02
Product NDC 81208-206
11-digit billing NDC 81208020602
UNII V06SV4M95S, 5A68WGF6WM, G63QQF2NOX, 4X49Y0596W
UPC 0850051361076
Application # M020
SPL Set ID 46465db7-c1f0-6980-e063-6294a90a3ed8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-04-30
Route TOPICAL
Dosage form GEL
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 81208-206-02 — 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 → 81208-0206-02. 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.

🏭 Manufacturer & labeler

LabelerYB CHEMIA LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code81208
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio2 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.

🩺 Clinical

🧪 What is this product?

This is a topical gel sunscreen marketed as an over-the-counter product under the FDA monograph rules for sunscreens. It contains four UV-filtering ingredients: avobenzone, homosalate, octisalate, and octocrylene, which are commonly used together to absorb and scatter ultraviolet light from the sun. The product is formulated as a gel intended for application to the skin to help reduce sun exposure. Sunscreen products of this type are typically used to help protect skin from UV radiation.

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.

💊 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.

  • UNII A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII 49ZWR266MZ
    A synthetic peptide fragment used as a conditioning agent and skin-softening ingredient in topical formulations. It helps improve texture and feel of creams or lotions.
  • 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 ZRA72DR3R7
    A waxy substance made from fatty acids and glycerin that acts as a binder and lubricant in tablets and capsules. It helps hold ingredients together and makes the medicine easier to swallow.
  • UNII N7YC58165T
    A synthetic polymer made from glycerin and sebacic acid, used as a film-former and binder in medications. It helps hold tablet or capsule ingredients together and may coat the product for controlled release.
  • UNII 8TY5YO42NJ
    Capryloyl glycine is a mild, skin-conditioning ingredient made from a natural fatty acid and the amino acid glycine. In medicines, it acts as a surfactant and preservative booster, helping the product spread evenly and resist contamination.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • 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 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 62ZVN02QZG
    A mushroom-derived ingredient used as a filler and binder in capsules and tablets. It helps hold the medicine together and adds bulk to the formulation.
  • UNII 609A3V1SUA
    A silky liquid derived from caprylic acid that acts as an emollient and solvent in formulations. It helps dissolve active ingredients and improves the spreadability and feel of lotions, creams, and topical products.
  • UNII W8CS8KBY2B
    A silicone-based polymer that forms a protective barrier on skin or mucous membranes. Used as an emollient and skin protectant in topical products to reduce moisture loss and create a smooth texture.
  • UNII O4I3UFO6ZF
    A silicone-based polymer blend that acts as an emulsifier and texture modifier. It helps keep oil and water mixed together in the formulation and gives the product a smooth, spreadable consistency.
  • UNII S3KFG6Q5X8
    An organic chemical compound used as a UV filter in topical formulations. It helps protect the medicine or product from degradation caused by sunlight exposure during storage and use.
  • 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 J5P04QW0CF
    A fungus used as a filler and natural colorant in supplements and medicines. It may help standardize the product's appearance and texture while adding bulk.
  • 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 O238UC53ET
    Grifola frondosa (maitake mushroom) is a fungal ingredient used as a filler and nutritional component in supplements and medicines to add bulk and support product formulation.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • 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 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 834K0WOS5G
    A natural fat extracted from sunflower seeds. It acts as an emulsifier and lubricant in medicines, helping mix ingredients that don't normally blend together and allowing the product to flow smoothly during manufacturing.
  • UNII 3HH93SL2H9
    A plant-derived oil made from meadowfoam seeds. It acts as an emollient and lubricant in medicines, helping soften formulations and improve how ingredients mix together.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII 5LKW3C543X
    A synthetic oily liquid derived from neopentyl glycol and heptanoic acid. It serves as an emollient and solvent in formulations, helping to dissolve or suspend active ingredients and improve the texture and spreadability of topical products.
  • UNII X8725R883T
    A synthetic oily liquid derived from branched carboxylic acids, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII 8Q1GYP08KU
    A fungus that grows on caterpillars in high-altitude regions, used in traditional medicine formulations. It may serve as an active botanical ingredient rather than a typical inactive excipient.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • UNII MGE3733FR2
    Polyglutamic acid is a synthetic polymer made from linked amino acids. In medications, it acts as a binder to hold tablet ingredients together and may help control how quickly the drug dissolves and releases in your body.
  • UNII Z570VEV8XK
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles so the medicine flows smoothly during manufacturing and remains free-flowing in the bottle.
  • UNII FO6B1S7BZU
    A plant extract from alpine rhododendron used as a natural colorant and antioxidant in medicines. It helps preserve the product and may provide a reddish or brown tint to tablets or capsules.
  • UNII 6W9PS8B71J
    Sorbitan monolaurate is a natural oil-derived emulsifier made from sorbitol and lauric acid. It helps mix oils and water-based ingredients together in the medicine so the formula stays uniform and smooth.
  • UNII S8R4V700NK
    A natural plant extract from terminalia chebula fruit, used in traditional medicine formulations. It may serve as a binder, natural colorant, or astringent agent to help hold tablet ingredients together or adjust product texture.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • UNII KM7N50LOS6
    Tin oxide is an inorganic mineral compound used in medicines as a colorant and opacifying agent. It provides white or off-white color to tablets, capsules, and coatings while helping make formulations less transparent.
  • UNII 4D20464K2J
    A synthetic compound derived from undecylenic acid combined with the amino acid glycine. It functions as a preservative and antimicrobial agent to help prevent contamination and extend the product's shelf life.
  • 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.

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

The official label also statesAcetyl Hexapeptide-1, C12-15 Alkyl Benzoate, C18-36 Acid Glycol Ester, C18-36 Acid Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Capryloyl Glycine, Caprylyl Glycol, Coprinus Comatus (Mushroom) Extract, Cordyceps Sinensis Extract, Dicaprylyl Carbonate, Dimethicone Crosspolymer-3, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Ethylhexyl Methoxycrylene, Ethylhexylglycerin, Ganoderma Lucidum (Reishi Mushroom) Extract, Glycerin, Grifola Frondosa (Mushroom) Extract, Isododecane, Isohexadecane, Isopropyl Palmitate, Lecithin, Meadowfoam Estolide, Neopentyl Glycol Diheptanoate, Octyldodecyl Neopentanoate, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Polyglutamic Acid, Polymethylsilsesquioxane, Rhododendron Ferrugineum Extract, Sorbitan Laurate, Terminalia Chebula (Haritaki) Fruit Extract, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Undecylenoyl Glycine, Water. May contain: Calcium Sodium Borosilicate, Iron Oxides, Mica, Synthetic Fluorphlogopite and Titanium Dioxide.

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Le Mieux Naked Glow Bronzer SPF 50 8 g/100g; 4 g/100g; 3 g/100g; 5 g/100gthis 81208-0206-02 YB 1 tube — — 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

🏛️
2025
On the market since
Apr 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
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.

🔬 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 Le Mieux Naked Glow Bronzer SPF 50 (this brand).

Top reported reactions

Rash13
Acne10
Sunburn9
Dry Skin8
Erythema8
Malignant Melanoma8
Headache7

Age at onset

Child1
Adult9
Elderly11

Reporter sex

139 reports
Male · 35%
Female · 65%

Serious outcomes

Hospitalization22
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 7 1
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
81208-0206-02 You're viewing this 1 TUBE in 1 CARTON (81208-206-02) / 50 g in 1 TUBE 2025-04-30 Active

🧭 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 FDA registers it as 81208-206-02, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 81208-0206-02, written without dashes as 81208020602. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 81208-0206-02, the first segment (81208) is the labeler code FDA assigned to YB CHEMIA LLC; the middle segment (0206) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
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 YB CHEMIA LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
YB CHEMIA LLC 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.

📄 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
🎯 Indications and Usage 31 words ▾

INDICATIONS & USAGE Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 82 words ▾

DIRECTIONS Apply liberally 15 minutes before sun exposure Rub in well. Reapply at least every 2 hours Children under 6 months: Ask a doctor Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially 10 a.m. to 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses.

⚠️ Warnings 35 words ▾

WARNINGS For external use only Do not use on damaged or broken skin Stop use and ask a doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove.

🧪 Active Ingredient 24 words ▾

ACTIVE INGREDIENTS Drug Facts Active Ingredients ……………….….. Purpose Avobenzone 3.0% ………………...... Sunscreen Homosalate 8.0% …………….......… Sunscreen Octisalate 5.0% ……………..........… Sunscreen Octocrylene 4.0% …………….......... Sunscreen

🧪 Inactive Ingredients 98 words ▾

INACTIVE INGREDIENTS Acetyl Hexapeptide-1, C12-15 Alkyl Benzoate, C18-36 Acid Glycol Ester, C18-36 Acid Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Capryloyl Glycine, Caprylyl Glycol, Coprinus Comatus (Mushroom) Extract, Cordyceps Sinensis Extract, Dicaprylyl Carbonate, Dimethicone Crosspolymer-3, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Ethylhexyl Methoxycrylene, Ethylhexylglycerin, Ganoderma Lucidum (Reishi Mushroom) Extract, Glycerin, Grifola Frondosa (Mushroom) Extract, Isododecane, Isohexadecane, Isopropyl Palmitate, Lecithin, Meadowfoam Estolide, Neopentyl Glycol Diheptanoate, Octyldodecyl Neopentanoate, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Polyglutamic Acid, Polymethylsilsesquioxane, Rhododendron Ferrugineum Extract, Sorbitan Laurate, Terminalia Chebula (Haritaki) Fruit Extract, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Undecylenoyl Glycine, Water.

May contain: Calcium Sodium Borosilicate, Iron Oxides, Mica, Synthetic Fluorphlogopite and Titanium Dioxide.

🎯 Purpose 29 words ▾

USES Helps prevent sunburn If used as directed, with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 81208-0203-02 · YB 81260-0001-20 · Dalton →
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.