Home › NDC Lookup › Ingredients › Octinoxate, Octocrylene, Octisalate, And... › 70325-3003-01
bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural Citrus Scent OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL Spray, 30 mL — NDC 70325-3003-01 package photo

bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural Citrus Scent OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL Spray, 30 mL

by Bu Brands, LLC · 30 mL in 1 BOTTLE, PLASTIC (70325-3003-1)
NDC 70325-3003-01
🏷️ FDA NDC (as labeled) 70325-3003-1 billing pads the package segment with a zero
This package
Contains30 mL Pack sizes2 compare ↓
Also comes in: 98 ml 70325-3003-03
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) 70325-3003-1
Product NDC 70325-3003
11-digit billing NDC 70325300301
UNII 4Y5P7MUD51, 5A68WGF6WM, 4X49Y0596W, G63QQF2NOX
UPC 0370325000062
Application # M020
SPL Set ID 9ac92c96-5bcf-421d-9cd0-73ddfa10195c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-12-01
Route TOPICAL
Dosage form SPRAY
Substance OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Why two NDCs? The FDA registers this code as 70325-3003-1 — 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 → 70325-3003-01. 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.

🏭 Manufacturer & labeler

LabelerBu Brands, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code70325
First marketedDec 2016
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?

This is a topical spray sunscreen formulated with four active UV-filtering ingredients: avobenzone, octinoxate, octisalate, and octocrylene. These chemical filters are commonly combined in sunscreens to absorb ultraviolet radiation and are typically applied to skin to help protect against sun damage. The product is labeled as broad-spectrum SPF 30 and alcohol-free, marketed as an over-the-counter monograph drug under FDA sunscreen regulations.

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 36HQN158VC
    Alpha-bisabolol is a naturally derived oily liquid from plant sources. It works as a fragrance, flavor, and skin-conditioning agent in topical medicines and cosmetic products.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • 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 CL439Y041G
    Davana oil is a fragrant plant-derived oil used as a flavoring agent and fragrance component in medications. It adds taste and aroma to make medicines more pleasant to take.
  • UNII I445L28B12
    A silicone-based compound that acts as a lubricant and glidant in tablet and capsule formulations. It reduces friction between particles and on equipment surfaces, helping medicines flow smoothly during manufacturing and tablet compression.
  • 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 AKN3KSD11B
    Orange oil obtained by cold pressing orange peel. It serves as a flavoring agent and fragrance in medicines to improve taste and aroma.
  • 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 KFR5QEN0N9
    A synthetic plastic polymer that helps form a protective film coating on the medicine. It's used as a binder and film-former to hold the tablet or capsule together and control how quickly the drug dissolves.

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

The official label also statesCyclopentasiloxane, Octyl Palmitate, Butyloctyl Salicylate, Diphenylsiloxy Phenyl Trimethicone, VP/Hexadecene Copolymer, Tocopherols, Bisabolol, Artemisia Pallens Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil.

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.
Try another pack size: 98 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
Kinesys 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 61481-3006-01 Wilc 30 ml — — FDA listed —
bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural Citrus Scent 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mLthis 70325-3003-01 Bu 30 ml — — FDA listed —
bu SPF 30 Broad Spectrum on Alcohol-Free Performance Sunscreen - Fragrance Free 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 70325-3001-01 Bu 30 ml — — FDA listed —
bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural White Sage Scent 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 70325-3002-01 Bu 30 ml — — FDA listed —
Kinesys Broad Spectrum SPF 30 Alcohol-Free Performance Sunscreen - Fragrance Free 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 61481-3001-01 Wilc 30 ml — — FDA listed —
Kinesys Broad Spectrum SPF 30 Kids Alcohol-Free Sunscreen 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 61481-3002-01 Wilc 30 ml — — FDA listed —
Kinesys Broad Spectrum SPF 30 Alcohol-Free Sunscreen - Mango Scent 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL 61481-3003-01 Wilc 30 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

🏛️
2016
On the market since
Dec 2016
📍
2026
Currently FDA-listed
10 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
70325-3003-01 You're viewing this 30 mL in 1 BOTTLE, PLASTIC (70325-3003-1) 2016-12-01 Active
70325-3003-03 98 mL in 1 BOTTLE, SPRAY (70325-3003-3) 2016-12-01 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 70325-3003-01?
NDC 70325-3003-01 contains 30 mL — 30 ml in 1 bottle, plastic.
What is the difference between NDC 70325-3003-01 and NDC 70325-3003-03?
Both are bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural Citrus Scent OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL Spray — the drug itself is identical. NDC 70325-3003-01 is the 30 mL package, while NDC 70325-3003-03 is the 98 ml package.
What NDC number is used to bill for this package of bu SPF 30 Broad Spectrum Alcohol-Free Performance Sunscreen - Natural Citrus Scent OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE 7.5 g/100mL; 7.5 g/100mL; 5 g/100mL; 2.5 g/100mL Spray?
Bill NDC 70325-3003-01 — the 11-digit billing format is 70325300301. 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 70325-3003-1, 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: 70325-3003-01, written without dashes as 70325300301. 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 70325-3003-01, the first segment (70325) is the labeler code FDA assigned to Bu Brands, LLC; the middle segment (3003) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Bu Brands, LLC. 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 1 other package presentation of this same product, including 98 ml (70325-3003-03). 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?
Bu Brands, LLC 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 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 107 words ▾

Directions apply liberally 15 minutes before sun exposure reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Do not spray directly onto the face. Spray into hands, and apply to the face. children under 6 months: 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 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

⚠️ Warnings 64 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 product is swallowed, get medical help or contact a Poison Control Center right away. Do not use near flame or while smoking

📦 Storage and Handling 11 words ▾

Other Information protect this product from excessive heat and direct sun

🧪 Active Ingredient 10 words ▾

Active Ingredients Octinoxate 7.50% Octocrylene 7.50% Octisalate 5.00% Avobenzone 2.50%.

🧪 Inactive Ingredients 24 words ▾

Inactive Ingredients Cyclopentasiloxane, Octyl Palmitate, Butyloctyl Salicylate, Diphenylsiloxy Phenyl Trimethicone, VP/Hexadecene Copolymer, Tocopherols, Bisabolol, Artemisia Pallens Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil.

🎯 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 ↗
← 70325-3002-01 · Bu 70329-0717-01 · STL →
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.