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Josie Maran Argan Daily Moisturizer SPF47 Zinc Oxide, Titanium Dioxide 6.4 mg/100mL; 5.1 mg/100mL Lotion, 60 mL — NDC 51514-0332-03 package photo

Josie Maran Argan Daily Moisturizer SPF47 Zinc Oxide, Titanium Dioxide 6.4 mg/100mL; 5.1 mg/100mL Lotion, 60 mL

by Autumn Harp, Inc. · 60 mL in 1 TUBE (51514-0332-3)
NDC 51514-0332-03
🏷️ FDA NDC (as labeled) 51514-0332-3 billing pads the package segment with a zero
This package
Contains60 mL Pack sizes4 compare ↓
Also comes in: 5 ml 51514-0332-01 15 ml 51514-0332-02 120 ml 51514-0332-04
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 51514-0332-3
Product NDC 51514-0332
11-digit billing NDC 51514033203
UNII SOI2LOH54Z, 15FIX9V2JP
Application # M020
SPL Set ID 027821e6-db7d-4c03-956a-00313488ebc7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-01-09
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 51514-0332-3 — 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 → 51514-0332-03. 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

LabelerAutumn Harp, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code51514
First marketedJan 2014
Product typeHuman Otc Drug
Portfolio3 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?

Josie Maran Argan Daily Moisturizer SPF47 is a topical lotion containing two mineral sunscreen active ingredients: zinc oxide and titanium dioxide. These ingredients are typically used together as physical UV filters to protect skin from ultraviolet radiation. This product is marketed as an over-the-counter sunscreen lotion under FDA's monograph rules for the sunscreen drug category.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

💊 What it looks like

FlavorMint
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII WC51CA3418
    A fragrance compound derived from cinnamon, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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 269CJD5GZ9
    A natural fruit extract from apricots used as a flavoring and coloring agent in medicines. It provides taste and visual appeal to make the medication more pleasant to take.
  • UNII 4V59G5UW9X
    Argan oil is a plant-derived oil from argan tree kernels. It's used in medicines as an emollient and skin-conditioning agent to help soften and moisturize the product's texture.
  • 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 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • 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 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • 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 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 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 OAH19558U1
    A synthetic compound made from coconut oil, laureth-12 helps mix oil and water-based ingredients together. It acts as an emulsifier and surfactant in formulations, improving how the medicine spreads and is absorbed.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII 9MC3I34447
    A natural oil extracted from citrus peel, used as a flavoring agent and solvent to improve taste and help dissolve or distribute other ingredients in the medicine.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII 6777U11MKT
    A silicone-based lubricant and anti-foaming agent used to reduce surface tension and prevent foam formation during manufacturing and storage of the medication.
  • 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 MPJ2Q8WI8G
    A plant-derived emulsifier made from glycerin and lauric acid. It helps mix oil and water-based ingredients together and improves product texture and stability in formulations.
  • UNII 062SZD3F3X
    A synthetic emulsifier made from glycerin and oleic acid. It helps blend oil and water-based ingredients together in formulations, keeping them evenly mixed throughout the product.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • UNII F8DRP5BB29
    A silicone-based polymer that acts as an emulsifier and skin-conditioning agent. It helps blend oil and water ingredients together and improves the texture and feel of topical formulations.
  • 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 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesAqua (Water)**, Ethylhexyl Palmitate, Caprylic/Capric Triglyceride**, Aloe Barbadensis Leaf Juice*, Polyglyceryl-6 Polyricinoleate**, Cyclopentasiloxane, Polysilicone-11, Argania Spinosa (Argan) Kernel Oil**, Glycerin**, Cera Alba (Beeswax)*, Coco-Caprylate/Caprate, Phenoxyethanol, Polyhydroxystearic Acid, Methicone, Alumina, Tocopheryl Acetate, Sodium Chloride**, Triethoxycaprylylsilane, Polyglyceryl-10 Laurate, Parfum (Fragrance)**, Bisabolol, Dimethicone, Simmondsia Chinensis (Jojoba) Seed Oil*, Laureth-12, Ethylhexylglycerin, Camellia Sinensis (Green Tea) Leaf Extract*, Citric Acid**, Potassium Sorbate**, Sodium Benzoate**. *ORGANIC **NATURAL

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: 5 ml 15 ml 120 ml
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
Josie Maran Argan Daily Moisturizer SPF47 6.4 mg/100mL; 5.1 mg/100mLthis 51514-0332-03 Autumn 60 ml — — 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

🏛️
2014
On the market since
Jan 2014
📍
2026
Currently FDA-listed
12 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Zinc Oxide, Titanium Dioxide — the ingredient across all brands.

Top reported reactions

Chemical Burn1
Condition Aggravated1
Dehydration1
Erythema1
Erythema Of Eyelid1
Eyelid Irritation1
Eyelid Oedema1

Reporter sex

3 reports
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
51514-0332-01 5 mL in 1 TUBE (51514-0332-1) 2014-01-24 Active
51514-0332-02 15 mL in 1 TUBE (51514-0332-2) 2014-01-24 Active
51514-0332-03 You're viewing this 60 mL in 1 TUBE (51514-0332-3) 2014-01-24 Active
51514-0332-04 120 mL in 1 TUBE (51514-0332-4) 2014-01-24 Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 51514-0332-03?
NDC 51514-0332-03 contains 60 mL — 60 ml in 1 tube.
What is the difference between NDC 51514-0332-03 and NDC 51514-0332-01?
Both are Josie Maran Argan Daily Moisturizer SPF47 Zinc Oxide, Titanium Dioxide 6.4 mg/100mL; 5.1 mg/100mL Lotion — the drug itself is identical. NDC 51514-0332-03 is the 60 mL package, while NDC 51514-0332-01 is the 5 ml package.
What NDC number is used to bill for this package of Josie Maran Argan Daily Moisturizer SPF47 Zinc Oxide, Titanium Dioxide 6.4 mg/100mL; 5.1 mg/100mL Lotion?
Bill NDC 51514-0332-03 — the 11-digit billing format is 51514033203. 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 51514-0332-3, 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: 51514-0332-03, written without dashes as 51514033203. 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 51514-0332-03, the first segment (51514) is the labeler code FDA assigned to Autumn Harp, Inc.; the middle segment (0332) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Autumn Harp, Inc.. 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 3 other package presentations of this same product, including 5 ml (51514-0332-01), 15 ml (51514-0332-02), 120 ml (51514-0332-04). 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?
Autumn Harp, 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.

📄 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.
🚨 Boxed Warning 🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings and Cautions ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🚨 Boxed Warning 2 words ▾

Drug Facts

🎯 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 3 words ▾

Apply as needed

⚠️ Warnings and Cautions 58 words ▾

Warnings For external use only Do not use on damaged or broken skin. Stop use and ask a doctor if rash occurs. When using this product · keep out of eyes · rinse with water to remove Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

⚠️ Warnings 20 words ▾

For external use only Do not use on damaged or broken skin When using this product, keep out of eyes

🧪 Active Ingredient 8 words ▾

Active Ingredients Zinc Oxide 6.4%** Titanium Dioxide 5.1%**

🧪 Inactive Ingredients 63 words ▾

Inactive Ingredients: Aqua (Water)**, Ethylhexyl Palmitate, Caprylic/Capric Triglyceride**, Aloe Barbadensis Leaf Juice*, Polyglyceryl-6 Polyricinoleate**, Cyclopentasiloxane, Polysilicone-11, Argania Spinosa (Argan) Kernel Oil**, Glycerin**, Cera Alba (Beeswax)*, Coco-Caprylate/Caprate, Phenoxyethanol, Polyhydroxystearic Acid, Methicone, Alumina, Tocopheryl Acetate, Sodium Chloride**, Triethoxycaprylylsilane, Polyglyceryl-10 Laurate, Parfum (Fragrance)**, Bisabolol, Dimethicone, Simmondsia Chinensis (Jojoba) Seed Oil*, Laureth-12, Ethylhexylglycerin, Camellia Sinensis (Green Tea) Leaf Extract*, Citric Acid**, Potassium Sorbate**, Sodium Benzoate**. *ORGANIC **NATURAL

🎯 Purpose 3 words ▾

Purpose Sunscreen Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 51511-0599-12 · ASO 51514-0337-01 · Autumn →
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.