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Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/g Lotion, 946 g — NDC 61973-0101-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/g Lotion, 946 g — NDC 61973-101-08 (Billing 61973-0101-08)

by Arizona Sun Products · 946 g in 1 BOTTLE

This is a package of 946 g of Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/g Lotion from Arizona Sun Products, marketed since Feb 2024 and currently FDA-listed.

NDC 61973-0101-08
🏷️ FDA NDC (as labeled) 61973-101-08 billing pads the product segment with a zero
This package
Contains946 g Pack sizes4 compare ↓
Product page 61973-0101-01 Also comes in: 30 g 61973-101-01 90 g 61973-101-03 120 g 61973-101-04
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 61973-101-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
61973 labeler · 101 product · 08 package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0711552311703
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61973-101-08
Product NDC 61973-101
11-digit billing NDC 61973010108
UNII 4X49Y0596W, G63QQF2NOX, 95OOS7VE0Y, 4Y5P7MUD51
UPC 0711552311703
Application # M020
SPL Set ID 10cd4a29-0139-9435-e063-6394a90a51a4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-07
Route TOPICAL
Dosage form LOTION
Substance OCTISALATE; AVOBENZONE; OXYBENZONE; OCTINOXATE
Why two NDCs? The FDA registers this code as 61973-101-08 — 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 → 61973-0101-08. 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?

Arizona Sun Sunscreen SPF15 is a lotion applied to skin to help protect against sun damage. It contains four active ingredients (avobenzone, octinoxate, octisalate, and oxybenzone) that function as ultraviolet (UV) filters, which are commonly used in sunscreen products to absorb or scatter UV radiation from the sun. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for sunscreen ingredients and labeling rather than being individually reviewed for approval.

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.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 30 g 90 g 120 g
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
61973-0101-08 You're viewing this 946 g in 1 BOTTLE 2024-02-07 — Active
61973-0101-01 61973-101-01 Main listing 30 g in 1 BOTTLE 2024-02-07 — Active
61973-0101-04 61973-101-04 120 g in 1 BOTTLE 2024-02-05 — Active
61973-0101-03 61973-101-03 90 g in 1 BOTTLE 2024-02-07 — Active

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

Pack size FAQ

What quantity is in this package?
This package contains 946 g — 946 g in 1 bottle.
How does this package differ from NDC 61973-0101-01?
Both are Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/g Lotion — the drug itself is identical. This page's package is the 946 g one, while NDC 61973-0101-01 is the 30 g package.
What NDC number is used to bill for this package of Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/g Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Arizona Sun Sunscreen SPF15 30 mg/g; 20 mg/g; 30 mg/g; 75 mg/gthis 61973-0101-08 Arizona 946 g — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2024
On the market since
Feb 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.

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

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 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 597E9BI3Z3
    Arctium lappa root is a plant-derived ingredient used in some traditional and herbal preparations. In formulations, it may serve as a natural extract or botanical agent to support product stability or flavor.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • 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 6V475AX06U
    A chelating agent derived from ethylenediaminetetraacetic acid (EDTA) combined with copper. It binds metals in formulations to prevent discoloration and degradation, helping preserve the medicine's stability and appearance.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII 01G73H6H83
    A plant extract from hop flowers, commonly used in brewing. In medicines, hops may serve as a flavoring agent or natural preservative to help maintain product stability.
  • UNII 39QC7B2817
    A natural ingredient derived from yellow lupin seeds. It acts as a binder and thickener, helping hold the medicine's ingredients together and give the product the right texture.
  • UNII 9936O846LI
    A plant extract from mullein leaves used as a natural flavoring agent and to add texture or body to liquid formulations. It may help improve the taste or mouthfeel of the medicine.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 81MCR2UQ6Q
    Rosa canina flower is a plant-derived ingredient from the wild rose plant. It's used in medicines as a natural flavoring agent and may also provide color or antioxidant properties to the formulation.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII II877K4UNR
    A plant extract from the night-blooming cereus flower, used as a natural flavoring or fragrance agent in medicines to improve taste or aroma.
  • UNII D24K2Q1F6H
    A plant oil extracted from jojoba seeds. It acts as an emollient and conditioning agent in topical formulations, helping soften skin and improve product texture and spreadability.
  • 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 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • UNII R9N3379M4Z
    Sunflower seed is a plant-derived ingredient used as a filler and source of oil in medications. It helps add bulk to the formulation and may serve as a natural binding or lubricating component.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII P83EQ521R3
    A plant extract from mistletoe berries used as a natural thickening agent and binder in medicines. It helps increase viscosity and hold tablet or capsule ingredients together.
  • UNII 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
  • 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 statesWater (Agua), Stearic Acid, Propylene Glycol, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosa Canina (Rose Hips) Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Verbascum Thapsus (Mullein) Extract, Lupinus Luteus Seed (Lupin) Extract, Humulus Lupulus (Hops) Extract, Cereus Grandiflorus (Cactus) Extract, Arctium Lappa (Burdock) Root Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Polysorbate 60, Cetearyl Alcohol, Carbomer, Glycerin, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance

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

LabelerArizona Sun Products
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code61973
First marketedFeb 2024
Product typeHuman Otc Drug
Portfolio21 products on file

More NDCs from Arizona Sun Products labeler code 61973

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📖 Instructions for Use 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses Provides minimal sunburn protection. Higher SPF gives more sunburn protection.

⏱️ Dosage and Administration 2 words ▾

Drug Facts

⚠️ Warnings 51 words ▾

Warnings For External use only. When using this product keep out of the eyes. Rinse with water to remove. Stop and ask a doctor if rash or irritation develps and lasts. Keep out of the reach of children If swallowed get medical help or contact a poison control center right away.

🧪 Active Ingredient 14 words ▾

Active Ingredients Ethylhexyl Methoxycinnamate (7.50%) Ethylhexyl Salicylate (3.00%) Benzophenone-3 (3.00%) Butyl Methoxydibenzoylmethane (Avobenzone) (2.00%)

🧪 Inactive Ingredients 82 words ▾

Inactive Ingredients Water (Agua), Stearic Acid, Propylene Glycol, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Rosa Canina (Rose Hips) Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Verbascum Thapsus (Mullein) Extract, Lupinus Luteus Seed (Lupin) Extract, Humulus Lupulus (Hops) Extract, Cereus Grandiflorus (Cactus) Extract, Arctium Lappa (Burdock) Root Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Polysorbate 60, Cetearyl Alcohol, Carbomer, Glycerin, Disodium EDTA, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Fragrance

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 When Using This Product 14 words ▾

When using this product keep out of the eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 12 words ▾

Stop and ask a doctor if rash or irritation develps and lasts.

📄 Keep Out of Reach of Children 20 words ▾

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

📄 Other Information 29 words ▾

Other Information Sun Alert: Limiting sun exposure, wearing protective clothing, and using suscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

📄 Questions or Comments 7 words ▾

Questions or Comments? Call toll free 1-800-442-4786

📖 Instructions for Use 42 words ▾

Directions Apply liberally and evenly to the skin 30 minutes before and during sun exposure. Reapply as needed or after towel drying, perspiring, swimming, and vigorous activities. Use on children under six months of age only wih the advise of a physician.

📄 Package Label / Principal Display Panel 1 words ▾

32ozspf15

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Sunscreen — the ingredient across all brands.

Top reported reactions

Macular Degeneration460
Pyrexia308
Nausea293
Pain289
Malaise265
Weight Decreased239
Therapeutic Product Effect Incomplete216

Reporter sex

0 reports

Serious outcomes

Death211
Life-threatening117
Disabling36
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 247 0
Most recent year is provisional (FAERS lags ~3 months).
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.

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 Arizona Sun Products. 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 30 g (61973-0101-01), 90 g (61973-0101-03), 120 g (61973-0101-04). 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?
Arizona Sun Products 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.
← 61973-0100-04 · Arizona 61973-0102-04 · Arizona →
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.