Home › NDC Lookup › Ingredients › Sunscreen › 61973-0111-04
Arizona Sun SPF 45 Golfblok Sunscreen 100 mg/g; 70 mg/g; 50 mg/g; 30 mg/g; 75 mg/g; 50 mg/g Spray, 120 g — NDC 61973-0111-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Arizona Sun SPF 45 Golfblok Sunscreen 100 mg/g; 70 mg/g; 50 mg/g; 30 mg/g; 75 mg/g; 50 mg/g Spray, 120 g — NDC 61973-111-04 (Billing 61973-0111-04)

by Arizona Sun Products · 120 g in 1 BOTTLE

This is a package of 120 g of Arizona Sun SPF 45 Golfblok Sunscreen 100 mg/g; 70 mg/g; 50 mg/g; 30 mg/g; 75 mg/g; 50 mg/g Spray from Arizona Sun Products, marketed since Feb 2024 and currently FDA-listed. It is this product's only package size.

NDC 61973-0111-04
🏷️ FDA NDC (as labeled) 61973-111-04 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 61973-111-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
61973 labeler · 111 product · 04 package
Package marketed since
Feb 21, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0711552446108
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61973-111-04
Product NDC 61973-111
11-digit billing NDC 61973011104
UNII V06SV4M95S, 5A68WGF6WM, 4X49Y0596W, G63QQF2NOX, 4Y5P7MUD51, 95OOS7VE0Y
UPC 0711552446108
Application # M020
SPL Set ID 11e74823-5956-4277-e063-6294a90a7e27
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-21
Route TOPICAL
Dosage form SPRAY
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE; OCTINOXATE; OXYBENZONE
Why two NDCs? The FDA registers this code as 61973-111-04 — 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 → 61973-0111-04. 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 SPF 45 Golfblok is a topical spray sunscreen marketed as an over-the-counter monograph product. It contains six active ingredients that function as ultraviolet light filters: avobenzone, homosalate, octinoxate, octisalate, octocrylene, and oxybenzone. These chemical absorbers are typically used to help protect skin from UV radiation. The spray formulation is intended for application to exposed skin surfaces.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
61973-0111-04 You're viewing this Main listing 120 g in 1 BOTTLE 2024-02-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Arizona Sun SPF 45 Golfblok Sunscreen 100 mg/g; 70 mg/g; 50 mg/g; 30 mg/g; 75 mg/g; 50 mg/gthis 61973-0111-04 Arizona 120 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 7LL6SY9YFV
    A synthetic polymer made from acrylic compounds. It forms a protective film coating on tablets or capsules to control how fast the medicine dissolves and releases in the digestive tract.
  • 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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII 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 6SO6U10H04
    Biotin is a B-vitamin used as a nutritional supplement in some medications. It may also serve as a colorant or marker in formulations.
  • 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 1BK9DDD24E
    A synthetic polymer made from propylene glycol and a crosslinking agent. It acts as a film-former and binder in medicines, helping create coatings on tablets or holding ingredients together in solid dosage forms.
  • 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 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 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.

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

The official label also statesSD Alcohol 40B, Acrylates/ Octylacrylamide Copolymer, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polyol Prepolymer 2, Panthenol, Simmondsia Chinensis (Jojoba) Seed Extract, Biotin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, Rosa Canina Flower (Rose Hips) 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 Root (Burdock) Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, 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 high sunburn protection. Higher SPF gives more sunburn protection

⏱️ Dosage and Administration 2 words ▾

Drug Facts

⚠️ Warnings 66 words ▾

Warnings For external use only. Do not swallow. Avoid contact with eyes. If contact occurs, rinse eyes thouroughly with water. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash or irritation develops and lasts. Keep out of the reach of children. If swallowed get medical help or contact a poison control center right away.

🧪 Active Ingredient 18 words ▾

Active Ingredients Homosalate (10.00%), Ethylhexyl Methoxycinnamate (7.50%), Octocrylene (7.00%), Ethylhexyl Salicylate (5.00%), Benzophenone-3 (5.00%), Butyl Methoxydibenzoylmethane (Avobenzone) (3.00%)

🧪 Inactive Ingredients 75 words ▾

Inactive Ingredients SD Alcohol 40B, Acrylates/ Octylacrylamide Copolymer, Tocopheryl Acetate (Vitamin E), Retinyl Palmitate, Polyol Prepolymer 2, Panthenol, Simmondsia Chinensis (Jojoba) Seed Extract, Biotin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Allantoin, Rosa Canina Flower (Rose Hips) 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 Root (Burdock) Extract, Viscum Album (Mistletoe) Fruit Extract, Helianthus Annuus (Sunflower) Seed Extract, Fragrance

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 When Using This Product 13 words ▾

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

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if rash or irritation develops 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 54 words ▾

Directions Apply liberally and evenly to the skin 30 minutes before and during sun exposure. Spray into hands and apply to the face. Avoid contact with eyes. 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 ▾

Golfblok

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

Age at onset

Neonate5
Infant8
Child29
Adolescent7
Adult120
Elderly203

Reporter sex

2,107 reports
Male · 36%
Female · 64%
Unknown · 0%

Serious outcomes

Death211
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 279 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.
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.
← 61973-0110-04 · Arizona 61973-0112-04 · 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.