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Everyday Coverage Tinted Sunscreen - Extra Light Tint Zinc Oxide 200 mg/mL Cream, 60 mL — NDC 72592-0001-60 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Everyday Coverage Tinted Sunscreen - Extra Light Tint Zinc Oxide 200 mg/mL Cream, 60 mL — NDC 72592-001-60 (Billing 72592-0001-60)

by MV Advanced · 60 mL in 1 BOTTLE, PUMP

This is a package of 60 mL of Everyday Coverage Tinted Sunscreen - Extra Light Tint Zinc Oxide 200 mg/mL Cream from MV Advanced, marketed since Sep 2010 and currently FDA-listed. It is this product's only package size.

NDC 72592-0001-60
🏷️ FDA NDC (as labeled) 72592-001-60 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 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

NDC database record

One package, one record: these facts belong to NDC 72592-001-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72592 labeler · 001 product · 60 package
Package marketed since
Sep 1, 2010
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7259200160 5
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72592-001-60
Product NDC 72592-001
11-digit billing NDC 72592000160
UNII SOI2LOH54Z
Application # M020
SPL Set ID 7834c649-5f6d-b005-e053-2a91aa0a1084
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-09-01
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 72592-001-60 — 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 → 72592-0001-60. 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?

This is a tinted sunscreen cream applied to the skin to help protect against sun damage. It contains zinc oxide, a mineral ingredient that functions as a physical sunscreen by reflecting and scattering ultraviolet rays away from the skin. The product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established safety and use rules for sunscreen products in this category. The extra light tint is intended to blend with the skin while the sunscreen provides coverage.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
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
72592-0001-60 You're viewing this Main listing 60 mL in 1 BOTTLE, PUMP 2010-09-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lilikoi Mineral Defense Sport Sunscreen SPF 30 200 mg/mL 15751-3040-05 Eminence 1 tube — — FDA listed —
Eminence Tropical Vanilla Day Cream SPF 40 Sunscreen 200 mg/mL 15751-3500-01 Eminence 1 jar — — Discontinued —
Eminence Lilikoi Daily Defense Moisturizer SPF 40 Sunscreen 200 mg/mL 15751-3501-01 Eminence 1 jar — — FDA listed —
Eminence Bright Skin Moisturizer SPF 40 Sunscreen 200 mg/mL 15751-3503-01 Eminence 1 jar — — FDA listed —
Sport Broad Spectrum SPF50 Water Resistant 80 minutes Mineral Sunscreen UVA UVB Protection Stick 200 mg/mL 53675-0203-00 Aruba 30 ml — — FDA listed —
Broad Spectrum SPF50 Water Resistant (80 minutes) Mineral Sunscreen UVA UVB Protection Stick for Kids 200 mg/mL 53675-0205-00 Aruba 30 ml — — FDA listed —
THINKSPORT sunscreen SPF 50 200 mg/mL 60781-1001-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKSPORT Kids sunscreen SPF 50 200 mg/mL 60781-1002-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKBABY Baby Sunscreen SPF 50 200 mg/mL 60781-1003-03 thinkOperations,LLC 89 ml — — FDA listed —
Think Every Day Face Sunscreen SPF 30 200 mg/mL 60781-1011-01 thinkOperations,LLC 59 ml — — FDA listed —
Think Aloe and Tea Leaves Zinc oxide 200 mg/mL 60781-4698-01 thinkOperations,LLC 89 ml — — FDA listed —
Raw Elements Daily Moisturizer Broad Spectrum SPF30 200 mg/mL 70680-0305-00 Raw 80 ml — — FDA listed —
SUNNY Q Broad Spectrum SPF-30 200 mg/mL 81738-0138-00 Sunny 100.55 ml — — FDA listed —
TIGER BABY Baby Sunscreen SPF-50 200 mg/mL 82247-0278-00 BRICKELL 5 ml — — FDA listed —
JOYSPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0354-00 JOYSPRING 30 ml — — FDA listed —
JOY SPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0356-00 JOYSPRING 90 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 2w 200 mg/mL 76354-0471-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Super Shield Mineral Sunscreen SPF50 200 mg/mL 79265-7778-01 Babo 89 ml — — FDA listed —
GLC OG Natural Tinted SPF 30 Sunscreen 200 mg/mL 84747-0530-00 GUD 1 jar — — FDA listed —
Sun Bum 50 Mineral Sunscreen 1 OZ 200 mg/mL 69039-0797-01 Sun 30 ml — — FDA listed —
Everyday Coverage Tinted Sunscreen - Extra Light Tint 200 mg/mLthis 72592-0001-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 9w 200 mg/mL 76354-0474-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 14w 200 mg/mL 76354-0479-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 3N 200 mg/mL 76354-0480-01 e.l.f. 1 bottle — — FDA listed —
Dr. Mercola Broad Spectrum 200 mg/mL 71239-0787-23 Natural 236 ml — — FDA listed —
Vitamin C BB Beauty Balm Sheer Tint SFP 30 200 mg/mL 55560-0108-01 Andalou 1 tube — — FDA listed —
Everyday Coverage Tinted Sunscreen - Light Tint 200 mg/mL 72592-0002-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 12w 200 mg/mL 76354-0477-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 5N 200 mg/mL 76354-0481-01 e.l.f. 1 bottle — — FDA listed —
Derma E Vitamin C Weightless Moisturizer SPF 45 200 mg/mL 54108-0359-01 derma 1 bottle — — FDA listed —
Kypris Pot of Shade Heliotropic Broad Spectrum SPF 30 Sunscreen And Primer 200 mg/mL 70608-0001-01 Kypris 1 jar — — FDA listed —
Everyday Coverage Tinted Sunscreen - Medium Tint 200 mg/mL 72592-0003-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 13w 200 mg/mL 76354-0478-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color plus Correct Sheer Beige SPF 30 200 mg/mL 55560-0110-01 Andalou 1 tube — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 1C 200 mg/mL 76354-0470-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 11w 200 mg/mL 76354-0476-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 8N 200 mg/mL 76354-0483-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50 200 mg/mL 79265-8758-01 Babo 89 ml — — FDA listed —
Thinkbaby Clear Zinc SPF 30 200 mg/mL 60781-4175-03 thinkOperations,LLC 89 ml — — FDA listed —
Baby Bum Mineral 50 Sunscreen 200 mg/mL 69039-0686-00 Sun 88 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 4W 200 mg/mL 76354-0472-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 7N 200 mg/mL 76354-0482-01 e.l.f. 1 bottle — — FDA listed —
Perfecting BB Beauty Balm Natural Tint SPF 30 200 mg/mL 55560-0104-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 200 mg/mL 69039-0728-01 Sun 88 ml — — FDA listed —
Vivaiodays Sunscreen with Turmeric 200 mg/mL 71778-0002-01 5SENCO 100 ml — — FDA listed —
Ultra Violette Future Screen Broad Spectrum SPF 50 200 mg/mL 84803-0103-15 Grace 15 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 10w 200 mg/mL 76354-0475-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color Plus Correct Sheer Tan SPF 30 200 mg/mL 55560-0106-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 32 OZ 200 mg/mL 69039-0718-01 Sun 946 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 6w 200 mg/mL 76354-0473-01 e.l.f. 1 bottle — — 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

🏛️
2010
On the market since
Sep 2010
📍
2026
Currently FDA-listed
16 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.

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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII 54JB35T06A
    A natural oil extracted from apricot pits, used as an emollient and lubricant in topical products. It helps soften the skin and improves the texture and spreadability of creams and lotions.
  • UNII FB4Q52I9K2
    A synthetic chemical compound used in medicines as a preservative or antimicrobial agent. It helps prevent bacterial and fungal growth in liquid formulations and topical products.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 9M6AAX381U
    A plant extract from carrot seeds used as a natural flavoring, coloring, or aromatic agent in medications. It may also provide antioxidant properties to help preserve the product's stability.
  • UNII G7036X8B5H
    A dark iron compound that gives medicine its color. Used as a colorant in tablets and capsules to help identify the medication and make it visually distinctive.
  • 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII O97ZV7726K
    A fragrant plant oil extracted from helichrysum flowers, used primarily as a flavor and fragrance agent to make medicines more pleasant tasting or smelling.
  • UNII T53SBG6741
    A plant-based oil extracted from sea buckthorn seeds. It's used as an emollient and skin-conditioning agent to soften the medicine's texture and improve how it feels or spreads on skin.
  • 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 67GS9BGA2X
    Labdanum oil is a resinous plant extract obtained from rockrose shrubs. In medicines, it functions as a fragrance, flavor agent, and emollient to improve product texture and palatability.
  • 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 412ZHA4T4Y
    A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
  • 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 A75L5FZ40U
    A natural colorant derived from freshwater pearl shells. It's used to give tablets and capsules a white or iridescent appearance and shine.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 9S8867952A
    A plant-derived oil from raspberry seeds used as an emollient and skin-conditioning agent in topical formulations. It helps soften the product texture and improve skin feel.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • 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.

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

The official label also statesCamellia Sinensis (Green Tea) Leaf Infusion, Helianthus Annuus (Sunflower) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Prunus Armeniaca (Apricot) Kernel Oil, Limnanthes Alba (Meadowfoam) Seed Oil, Vegetable Glycerin, Rubus Idaeus (Red Raspberry) Seed Oil, Mixed Tocopherols (Vitamin E), Polyaminopropyl Biguanide, Phospholipids (Soy Lecithin), Potassium Sorbate, Allantoin, Xanthan Gum, Citric Acid, Mica, Hippophae Rhamnoides (Sea Buckthorn) Oil, Rosmarinus Officinalis (Rosemary) Oleoresin, Pearl Powder, Iron Oxides, Daucus Carota Sativa (Carrot) Seed Extract, Cistus Ladaniferus (Cistus) Oil*, Helichrysum Italicum (Immortelle) Flower Oil* *Essential Oil

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

LabelerMV Advanced
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code72592
First marketedSep 2010
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from MV Advanced labeler code 72592

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 📋 Description 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 27 words ▾

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 101 words ▾

Shake well. Apply liberally to face/neck/chest 15 minutes before sun exposure (applying Protective Day Oil prior is highly recommended). Reapply at least every 2 hours.

Use a water-resistant sunscreen if swimming or sweating. Children under 6 months: consult a physician. Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging.

To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses.

⚠️ Warnings 30 words ▾

Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and consult a physician if rash occurs.

📦 Storage and Handling 12 words ▾

Protect the product in this container from excessive heat and direct sun.

🧪 Active Ingredient 6 words ▾

ACTIVE INGREDIENT: 20% non-nano zinc oxide

🧪 Inactive Ingredients 81 words ▾

Camellia Sinensis (Green Tea) Leaf Infusion, Helianthus Annuus (Sunflower) Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Prunus Armeniaca (Apricot) Kernel Oil, Limnanthes Alba (Meadowfoam) Seed Oil, Vegetable Glycerin, Rubus Idaeus (Red Raspberry) Seed Oil, Mixed Tocopherols (Vitamin E), Polyaminopropyl Biguanide, Phospholipids (Soy Lecithin), Potassium Sorbate, Allantoin, Xanthan Gum, Citric Acid, Mica, Hippophae Rhamnoides (Sea Buckthorn) Oil, Rosmarinus Officinalis (Rosemary) Oleoresin, Pearl Powder, Iron Oxides, Daucus Carota Sativa (Carrot) Seed Extract, Cistus Ladaniferus (Cistus) Oil*, Helichrysum Italicum (Immortelle) Flower Oil* *Essential Oil

🎯 Purpose 1 words ▾

Sunscreen

📋 Description 4 words ▾

marieveronique.com Made in California

📄 Package Label / Principal Display Panel 22 words ▾

Marie Veronique Everyday Coverage Tinted Sunscreen Broad Spectrum SPF 30 UVA/UVB Active Ingredient: Non-Nano Zinc Oxide 2 fl oz 60 mL 001

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 MV Advanced. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
MV Advanced 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.
← 72587-0003-01 · La 72592-0002-60 · MV →
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.