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Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2.5N Neutral OCTISALATE, TITANIUM DIOXIDE 51 mg/mL; 48 mg/mL Emulsion — NDC 61957-3706-00 package photo

Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2.5N Neutral OCTISALATE, TITANIUM DIOXIDE 51 mg/mL; 48 mg/mL Emulsion

by Parfums Christian Dior · 1 BOTTLE in 1 CARTON (61957-3706-0) / 40 mL in 1 BOTTLE
NDC 61957-3706-00
🏷️ FDA NDC (as labeled) 61957-3706-0 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 3, 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) 61957-3706-0
Product NDC 61957-3706
11-digit billing NDC 61957370600
UNII 4X49Y0596W, 15FIX9V2JP
Application # M020
SPL Set ID be60feb0-8c16-4ef6-a36f-423ed18e098c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-01
Route TOPICAL
Dosage form EMULSION
Substance OCTISALATE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 61957-3706-0 — a 5-4-1 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 package segment → 61957-3706-00. 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

LabelerParfums Christian Dior
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code61957
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio224 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 tinted moisturizer emulsion applied to the skin that functions as a sunscreen product. It contains two active ingredients, octisalate and titanium dioxide, which are typically used together as ultraviolet light filters to help protect skin from sun exposure. The product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for sunscreen products rather than undergoing individual review. This type of product is commonly used to provide sun protection while also adding light color and moisture to the complexion.

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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII 7J5R5W72QM
    C9-12 alkane is a clear, colorless liquid hydrocarbon mixture derived from petroleum. In medicines, it serves as a solvent, lubricant, or component in liquid formulations to help dissolve or suspend active ingredients.
  • 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 8D9H4QU99H
    A synthetic fatty acid ester derived from coconut oil, used as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the body absorbs certain drugs.
  • 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 E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 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 9M44R3409A
    A modified corn starch where some starch molecules have hydroxypropyl groups attached. It's used as a binder and disintegrant to help hold tablet ingredients together and allow the tablet to break apart properly when swallowed.
  • 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 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII 9229XJ4V12
    A synthetic emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients in formulations, keeping them mixed and preventing separation.
  • UNII 46P231IQV8
    A synthetic emulsifier derived from glycerin and fatty acids. It helps blend oil and water-based ingredients together in cosmetic and pharmaceutical formulations to create stable, uniform products.
  • UNII SMD1X3XO9M
    Powdered cellulose is a fine, plant-based powder made from purified wood fibers. In medicines, it acts as a filler to add bulk and volume, and helps tablets or capsules hold together during manufacturing and storage.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • 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 OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII VU97D01BF9
    A waxy emulsifier derived from sorbitol, a natural sugar alcohol. It helps blend oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII OLX698AH5P
    A clay mineral processed with a quaternary ammonium compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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 A3LZF0L939
    Tridecane is a clear, colorless liquid hydrocarbon derived from petroleum. It acts as a solvent and lubricant in medicines, helping distribute active ingredients evenly and reducing friction during manufacturing and tablet compression.
  • UNII JV0QT00NUE
    Undecane is a clear liquid hydrocarbon derived from petroleum. It functions as a solvent and processing aid in medicines, helping dissolve or suspend active ingredients and improve how the drug is manufactured and delivered.
  • 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.

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

The official label also statesAQUA (WATER) • DICAPRYLYL CARBONATE • GLYCERIN • UNDECANE • PROPANEDIOL • ALCOHOL • POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE • CELLULOSE • C9-12 ALKANE • DIPROPYLENE GLYCOL • POLYGLYCERYL-3 DIISOSTEARATE • TRIDECANE • LECITHIN • SILICA • HYDROXYPROPYL STARCH • PARFUM (FRAGRANCE) • STEARALKONIUM HECTORITE • DEXTRIN ISOSTEARATE • COCO-CAPRYLATE/CAPRATE • ALUMINUM HYDROXIDE • SODIUM MYRISTORYLGL GLUTAMATE • SORBITAN SESQUIISOSTEARATE • SODIUM CITRATE • SODIUM BENZOATE • PROPYLENE CARBONATE • STEARIC ACID • ALUMINA • OCTYLDODECANOL • MICA • CITRIC ACID • TOCOPHEROL • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • PENTYLENE GLYCOL • COLLAGEN AMINO ACIDS. (MAY CONTAIN: CI 77163 (BISMUTH OXYCHLORIDE) • CI 77491 (IRON OXIDES) • CI 77492 (IRON OXIDES) • CI 77499 (IRON OXIDES) • cI 77891 (TITANIUM DIOXIDE) • CI 77947 (ZINC OXIDE)). N° 23674/Z

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 mLPer 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
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2W Warm 51 mg/mL; 48 mg/mL 61957-3709-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2N Neutral 51 mg/mL; 48 mg/mL 61957-3708-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1CR Cool Rosy 51 mg/mL; 48 mg/mL 61957-3703-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0.5N Neutral 51 mg/mL; 48 mg/mL 61957-3700-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2.5N Neutral 51 mg/mL; 48 mg/mLthis 61957-3706-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3.5N Neutral 51 mg/mL; 48 mg/mL 61957-3710-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3N Neutral 51 mg/mL; 48 mg/mL 61957-3712-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4W Warm 51 mg/mL; 48 mg/mL 61957-3716-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1.5N Neutral 51 mg/mL; 48 mg/mL 61957-3702-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4N Neutral 51 mg/mL; 48 mg/mL 61957-3715-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1W Warm 51 mg/mL; 48 mg/mL 61957-3705-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3CR Cool Rosy 51 mg/mL; 48 mg/mL 61957-3711-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4.5N Neutral 51 mg/mL; 48 mg/mL 61957-3714-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 0N Neutral 51 mg/mL; 48 mg/mL 61957-3701-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 1N Neutral 51 mg/mL; 48 mg/mL 61957-3704-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2CR Cool Rosy 51 mg/mL; 48 mg/mL 61957-3707-00 Parfums 1 bottle — — FDA listed —
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 3W Warm 51 mg/mL; 48 mg/mL 61957-3713-00 Parfums 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

🏛️
2026
On the market since
Sep 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
61957-3706-00 You're viewing this 1 BOTTLE in 1 CARTON (61957-3706-0) / 40 mL in 1 BOTTLE 2026-09-01 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 61957-3706-0, 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: 61957-3706-00, written without dashes as 61957370600. 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 61957-3706-00, the first segment (61957) is the labeler code FDA assigned to Parfums Christian Dior; the middle segment (3706) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 Parfums Christian Dior. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Parfums Christian Dior 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 ▾

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 91 words ▾

Directions Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating.

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 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-sleeve shirts, pants, hats, and sunglasses.

Children under 6 months of age: ask a doctor.

⚠️ Warnings 54 words ▾

Warnings 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 swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 9 words ▾

Active ingredients Octisalate 4.50% Titanium dioxide 4.23% Purpose Sunscreen

🧪 Inactive Ingredients 126 words ▾

Inactive ingredients AQUA (WATER) • DICAPRYLYL CARBONATE • GLYCERIN • UNDECANE • PROPANEDIOL • ALCOHOL • POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE • CELLULOSE • C9-12 ALKANE • DIPROPYLENE GLYCOL • POLYGLYCERYL-3 DIISOSTEARATE • TRIDECANE • LECITHIN • SILICA • HYDROXYPROPYL STARCH • PARFUM (FRAGRANCE) • STEARALKONIUM HECTORITE • DEXTRIN ISOSTEARATE • COCO-CAPRYLATE/CAPRATE • ALUMINUM HYDROXIDE • SODIUM MYRISTORYLGL GLUTAMATE • SORBITAN SESQUIISOSTEARATE • SODIUM CITRATE • SODIUM BENZOATE • PROPYLENE CARBONATE • STEARIC ACID • ALUMINA • OCTYLDODECANOL • MICA • CITRIC ACID • TOCOPHEROL • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • PENTYLENE GLYCOL • COLLAGEN AMINO ACIDS.

(MAY CONTAIN: CI 77163 (BISMUTH OXYCHLORIDE) • CI 77491 (IRON OXIDES) • CI 77492 (IRON OXIDES) • CI 77499 (IRON OXIDES) • cI 77891 (TITANIUM DIOXIDE) • CI 77947 (ZINC OXIDE)). N° 23674/Z

🎯 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 ↗
← 61957-3705-00 · Parfums 61957-3707-00 · Parfums →
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.