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Avene Multi-Defense Fluid Zinc oxide 120 mg/mL Lotion — NDC 64760-778-01 (Billing 64760-0778-01)

by Pierre Fabre USA Inc. · 1 TUBE in 1 CARTON / 40 mL in 1 TUBE

This is a package of Avene Multi-Defense Fluid Zinc oxide 120 mg/mL Lotion from Pierre Fabre USA Inc., marketed since May 2024 and currently FDA-listed. It is this product's only package size.

NDC 64760-0778-01
🏷️ FDA NDC (as labeled) 64760-778-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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 64760-778-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
64760 labeler · 778 product · 01 package
Package marketed since
May 1, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6476077801 3
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) 64760-778-01
Product NDC 64760-778
11-digit billing NDC 64760077801
UNII SOI2LOH54Z
Application # M020
SPL Set ID 1329e56d-1e74-4bcc-e063-6394a90ae0c3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-01
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 64760-778-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 64760-0778-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

Avene Multi-Defense Fluid is a topical lotion containing zinc oxide, an ingredient commonly used in over-the-counter sun protection products. Zinc oxide functions as a physical sunscreen agent that helps reflect ultraviolet light away from the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for sunscreen formulations rather than undergoing individual product review.

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
64760-0778-01 You're viewing this Main listing 1 TUBE in 1 CARTON / 40 mL in 1 TUBE 2024-05-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cetaphil Sheer Mineral Face Liquid Sunscreen SPF 50 120 mg/mL 00299-4110-00 Galderma 1 bottle — — FDA listed —
Personalized Day Moisturizer with SPF 120 mg/mL 73572-0003-30 Proven 30 ml — — FDA listed —
Personalized Day Moisturizer with SPF 50 120 mg/mL 73572-0007-01 Proven 30 ml — — FDA listed —
KISS MY FACE SPF-50 Baby Mineral Sunscreen 120 mg/mL 74154-0317-00 WINDMILL 118 ml — — FDA listed —
KISS MY FACE SPF-50 Daily Mineral Sunscreen 120 mg/mL 74154-0318-00 WINDMILL 118 ml — — FDA listed —
KISS MY FACE SPF-50 Face Factor Mineral Sunscreen 120 mg/mL 74154-0319-00 WINDMILL 59 ml — — FDA listed —
Halo Glow Skin Tint SPF 50 84513 120 mg/mL 76354-0559-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84514 120 mg/mL 76354-0560-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84520 120 mg/mL 76354-0666-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Alabaster 120 mg/mL 83249-0004-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Spice 120 mg/mL 83249-0013-01 Rms 1 bottle — — FDA listed —
Luminous Defense SPF 50 120 mg/mL 84163-0056-15 Levels 1 bottle — — FDA listed —
Guidance To Glow Tru Spf 35 120 mg/mL 84444-0506-00 GUIDANCE 1 tube — — FDA listed —
Avene Face Sunscreen SPF 50 120 mg/mL 64760-0782-01 Pierre 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84510 120 mg/mL 76354-0556-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84512 120 mg/mL 76354-0558-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84521 120 mg/mL 76354-0667-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Tawny 120 mg/mL 83249-0015-01 Rms 1 bottle — — FDA listed —
Avene Multi-Defense Fluid 120 mg/mLthis 64760-0778-01 Pierre 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Mocha 120 mg/mL 83249-0011-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Toffee 120 mg/mL 83249-0016-01 Rms 1 bottle — — FDA listed —
Halo Glow Skin Tint SPF 50 84515 120 mg/mL 76354-0561-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84518 120 mg/mL 76354-0664-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Honey 120 mg/mL 83249-0008-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Ivory 120 mg/mL 83249-0009-01 Rms 1 bottle — — FDA listed —
Halo Glow Skin Tint SPF 50 84504 120 mg/mL 76354-0550-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84508 120 mg/mL 76354-0554-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Tan 120 mg/mL 83249-0014-01 Rms 1 bottle — — FDA listed —
Avene Multi-Defense Fluid Tinted 120 mg/mL 64760-0779-01 Pierre 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84509 120 mg/mL 76354-0555-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84511 120 mg/mL 76354-0557-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF 50 84506 120 mg/mL 76354-0552-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Buff 120 mg/mL 83249-0005-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Cameo 120 mg/mL 83249-0006-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Mahogany 120 mg/mL 83249-0010-01 Rms 1 bottle — — FDA listed —
Halo Glow Skin Tint SPF 50 84507 120 mg/mL 76354-0553-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84516 120 mg/mL 76354-0662-01 e.l.f. 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84517 120 mg/mL 76354-0663-01 e.l.f. 1 tube — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Caramel 120 mg/mL 83249-0007-01 Rms 1 bottle — — FDA listed —
Rms Suncoverup Super Tint Spf 50 Sand 120 mg/mL 83249-0012-01 Rms 1 bottle — — FDA listed —
Bubble Solar Mate Daily Mineral Sunscreen SPF 40 120 mg/mL 83509-0156-01 Bubble 1 tube — — FDA listed —
Halo Glow Skin Tint SPF50 -84519 120 mg/mL 76354-0665-01 e.l.f. 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

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerPierre Fabre USA Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code64760
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio12 products on file

More NDCs from Pierre Fabre USA Inc. labeler code 64760

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 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 111 words ▾

Directions Adults and children 6 months and older: • Apply generously 15 minutes before sun exposure • Reapply: • at least every 2 hours • after 40 minutes of swimming or sweating • immediately after towel drying • Children under 6 months of age: Ask a doctor • 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. to 2 p.m. • Wear long-sleeve shirts, pants, hats, and sunglasses.

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 5 words ▾

Active ingredient Zinc Oxide 12%

🧪 Inactive Ingredients 57 words ▾

Inactive Ingredients Water, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Jojoba Esters, Propanediol, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Tridecyl Salicylate, Nylon-12, Niacinamide, Methylpropanediol, Silica, Glycerin, Sodium Chloride, Coco-Caprylate, Polyglyceryl-2 Dipolyhydroxystearate, Caprylyl Glycol, Bisabolol, Allantoin, Oryza Sativa (Rice) Bran Extract, Lecithin, Stearalkonium Hectorite, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Polyricinoleate, Phenylpropanol, Helianthus Annuus (Sun‑ower) Extract, Tocopherol, Rosmarinus Of­cinalis (Rosemary) Leaf Extract, Tetrasodium Glutamate Diacetate, Sodium Hydroxide.

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 7 words ▾

Do not use • on broken skin.

📄 Ask a Doctor Before Use If 10 words ▾

Stop use and ask a doctor if • rash occurs.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, call a poison control center or get medical help right away.

📄 Questions or Comments 3 words ▾

Questions? 1-866-41-AVENE (28363)

📄 Package Label / Principal Display Panel 4 words ▾

Box 338075 Box 338075

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Pierre Fabre USA Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Pierre Fabre USA Inc. 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.
← 64760-0777-01 · Pierre 64760-0779-01 · Pierre →
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.