Home › NDC Lookup › Ingredients › Octinoxate, Octisalate And Zinc Oxide › 70605-0029-07
Principal Secret Reclaim Botanical (with SP) Radiant Recovery Day Broad Spectrum SPF 15 Octinoxate, Octisalate, and Zinc Oxide 7.5 g/100g; 5 g/100g; 3 g/100g Cream, 15 g — NDC 70605-0029-07 package photo

Principal Secret Reclaim Botanical (with SP) Radiant Recovery Day Broad Spectrum SPF 15 Octinoxate, Octisalate, and Zinc Oxide 7.5 g/100g; 5 g/100g; 3 g/100g Cream, 15 g

by Guthy-Renker LLC · 15 g in 1 JAR (70605-029-07)
NDC 70605-0029-07
🏷️ FDA NDC (as labeled) 70605-029-07 billing pads the product segment with a zero
This package
Contains15 g Pack sizes2 compare ↓
Also comes in: 30 g 70605-0029-43
OTC On market Non-controlled
🗂️ Data synced Jul 24, 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) 70605-029-07
Product NDC 70605-029
11-digit billing NDC 70605002907
UNII 4Y5P7MUD51, 4X49Y0596W, SOI2LOH54Z
Application # M020
SPL Set ID 6437fbf6-c84b-497e-bf69-b20153d4c706
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-04-30
Route TOPICAL
Dosage form CREAM
Substance OCTINOXATE; OCTISALATE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 70605-029-07 — 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 → 70605-0029-07. 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

LabelerGuthy-Renker LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code70605
First marketedApr 2016
Product typeHuman Otc Drug
Portfolio8 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 an over-the-counter topical cream that functions as a daytime moisturizer with broad-spectrum sunscreen protection. The three active ingredients, octinoxate, octisalate, and zinc oxide, are all UV filters that work together to help protect skin from ultraviolet radiation. The product is marketed under FDA's OTC monograph rules for sunscreen and skincare products. It is intended for topical application to the skin.

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.

🧪 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 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 L4EL31FWIL
    A synthetic peptide (short chain of amino acids) used as a conditioning or texture-enhancing agent in topical formulations. It helps improve product feel and skin compatibility in creams and lotions.
  • UNII SMF2K46G8D
    A red algae extract used as a gelling agent and thickener in medicines. It forms a gel-like consistency that helps control how the medicine releases and is absorbed in the body.
  • 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 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 5077EL0C60
    A plant extract from camellia leaves used in formulations as an antioxidant and skin-conditioning agent. It helps protect the product and its active ingredients from degradation.
  • 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 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • 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 46L1B02ND9
    A synthetic fragrance ingredient derived from myrcene, a natural plant oil. It adds a fresh, woody scent to the medicine and helps mask unpleasant flavors or odors of active ingredients.
  • 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 SF2JS9GF5T
    Ethyl linalool is a fragrant compound commonly used as a flavoring or aromatic agent in medications. It provides pleasant taste or scent to make the medicine more acceptable to take.
  • 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 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 14170060AT
    A synthetic colorant used to give medicines their yellow, orange, or red appearance. It helps identify the drug and makes it visually distinctive.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII VYT2JA85NH
    A plant extract from cogon grass roots used in some formulations. It may serve as a natural filler, thickening agent, or ingredient to help bind tablet components together.
  • 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 24RS0A988O
    Lemon is a citrus fruit extract used as a natural flavoring agent and acidulant to add tart taste and help preserve medicines while improving their palatability.
  • UNII 5K47SSQ51G
    A fragrant compound found in plants like lavender and bergamot. It's used as a flavoring and aroma agent to improve the taste and smell of medications.
  • UNII DJO934BRBD
    A plant-derived substance from alfalfa used as a filler and nutritional ingredient in supplements and medicines. It adds bulk to tablets and capsules while providing fiber and trace nutrients.
  • UNII 3GW44CIE3Y
    A synthetic fragrance compound used to add pleasant scent to medicines. It helps mask unpleasant tastes or odors in oral products and may improve patient acceptance of the medication.
  • UNII 1MGA33DQ5R
    A synthetic fatty acid compound used as an emulsifier and skin-conditioning agent in topical formulations. It helps stabilize mixtures of oil and water-based ingredients and improves product texture and spreadability on skin.
  • UNII 1615WE9073
    This is a synthetic peptide-like compound used as an emulsifier and stabilizer in medications. It helps keep oil and water-based ingredients mixed together and maintains product consistency.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • 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 ML9LGA7468
    A naturally-derived alcohol used as a preservative and fragrance in medicines. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 5XB3A63Y52
    A synthetic rubber polymer used as a glidant and lubricant in tablet and capsule formulations. It reduces friction between particles and equipment surfaces, helping medicines flow smoothly during manufacturing and preventing sticking.
  • UNII YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • 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 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.
  • 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.

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

The official label also statesWater, Glycerin, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Jojoba Esters, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Imperata Cylindrica Root Extract, Acetyl Hexapeptide-8, Palmitoyl Dipeptide-5 Diaminobutyroyl Hydroxythreonine, Palmitoyl Dipeptide-5 Diaminohydroxybutyrate, Tetradecyl Aminobutyroylvalylaminobutyric Urea Trifluoroacetate, Sodium Hyaluronate, Tocopheryl Acetate, Panthenol, Medicago Sativa (Alfalfa) Extract, Hydrolyzed Myrtus Communis Leaf Extract, Ahnfeltia Concinna Extract, Glycosaminoglycans, Pseudoalteromonas Ferment Extract, Camellia Oleifera Leaf Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Hydrogenated Lecithin, Triethoxycaprylylsilane, Xanthan Gum, Polyisobutene, Polysorbate 20, Polyacrylate-13, Butylene Glycol, Ceteareth-20, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Ethylhexylglycerin, Caprylyl Glycol, Phenoxyethanol, Ethyl Linalool, Methyldihydrojasmonate, Linalyl Acetate, 2,6-Dimethyl-7-Octen-2-ol, Hexamethylindanopyran, Phenethyl Alcohol.

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.
Try another pack size: 30 g
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
Principal Secret Reclaim Botanical (with SP) Radiant Recovery Day Broad Spectrum SPF 15 7.5 g/100g; 5 g/100g; 3 g/100gthis 70605-0029-07 Guthy-Renker 15 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

🏛️
2016
On the market since
Apr 2016
📍
2026
Currently FDA-listed
10 years 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70605-0029-07 You're viewing this 15 g in 1 JAR (70605-029-07) 2016-04-30 Active
70605-0029-43 30 g in 1 JAR (70605-029-43) 2016-04-30 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 70605-0029-07?
NDC 70605-0029-07 contains 15 g — 15 g in 1 jar.
What is the difference between NDC 70605-0029-07 and NDC 70605-0029-43?
Both are Principal Secret Reclaim Botanical (with SP) Radiant Recovery Day Broad Spectrum SPF 15 Octinoxate, Octisalate, and Zinc Oxide 7.5 g/100g; 5 g/100g; 3 g/100g Cream — the drug itself is identical. NDC 70605-0029-07 is the 15 g package, while NDC 70605-0029-43 is the 30 g package.
What NDC number is used to bill for this package of Principal Secret Reclaim Botanical (with SP) Radiant Recovery Day Broad Spectrum SPF 15 Octinoxate, Octisalate, and Zinc Oxide 7.5 g/100g; 5 g/100g; 3 g/100g Cream?
Bill NDC 70605-0029-07 — the 11-digit billing format is 70605002907. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 70605-029-07, 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: 70605-0029-07, written without dashes as 70605002907. 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 70605-0029-07, the first segment (70605) is the labeler code FDA assigned to Guthy-Renker LLC; the middle segment (0029) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (07) 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 Guthy-Renker LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 30 g (70605-0029-43). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Guthy-Renker 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 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

⏱️ Dosage and Administration 30 words ▾

Directions apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months: Ask a doctor

⚠️ Warnings 91 words ▾

Warnings Skin Cancer/Skin Aging Alert Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging. For external use only Do not use on damaged or broken skin.

When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 11 words ▾

Other information protect this product from excessive heat and direct sun

🧪 Active Ingredient 9 words ▾

Active ingredients Octinoxate 7.5% Octisalate 5% Zinc Oxide 3.0%

🧪 Inactive Ingredients 100 words ▾

Inactive ingredients Water, Glycerin, Butyrospermum Parkii (Shea) Butter, C12-15 Alkyl Benzoate, Jojoba Esters, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Imperata Cylindrica Root Extract, Acetyl Hexapeptide-8, Palmitoyl Dipeptide-5 Diaminobutyroyl Hydroxythreonine, Palmitoyl Dipeptide-5 Diaminohydroxybutyrate, Tetradecyl Aminobutyroylvalylaminobutyric Urea Trifluoroacetate, Sodium Hyaluronate, Tocopheryl Acetate, Panthenol, Medicago Sativa (Alfalfa) Extract, Hydrolyzed Myrtus Communis Leaf Extract, Ahnfeltia Concinna Extract, Glycosaminoglycans, Pseudoalteromonas Ferment Extract, Camellia Oleifera Leaf Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Hydrogenated Lecithin, Triethoxycaprylylsilane, Xanthan Gum, Polyisobutene, Polysorbate 20, Polyacrylate-13, Butylene Glycol, Ceteareth-20, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Ethylhexylglycerin, Caprylyl Glycol, Phenoxyethanol, Ethyl Linalool, Methyldihydrojasmonate, Linalyl Acetate, 2,6-Dimethyl-7-Octen-2-ol, Hexamethylindanopyran, Phenethyl Alcohol.

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 70605-0028-95 · Guthy-Renker 70605-0042-43 · Guthy-Renker →
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.