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By the Beach Suncare SPF 30 Suncare Citrus Crush 10 mg/100mL; 3 mg/100mL; 5 mg/100mL Cream, 177 mL — NDC 87094-0111-12 package photo

By the Beach Suncare SPF 30 Suncare Citrus Crush 10 mg/100mL; 3 mg/100mL; 5 mg/100mL Cream, 177 mL

by By the Beach Suncare LLC · 177 mL in 1 TUBE (87094-111-12)
NDC 87094-0111-12
🏷️ FDA NDC (as labeled) 87094-111-12 billing pads the product segment with a zero
This package
Contains177 mL Pack sizes2 compare ↓
Also comes in: 118 ml 87094-0111-11
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) 87094-111-12
Product NDC 87094-111
11-digit billing NDC 87094011112
UNII 5A68WGF6WM, G63QQF2NOX, 4X49Y0596W
UPC 0860092001527
Application # M020
SPL Set ID 43918d25-e947-5e17-e063-6394a90ada7c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-10-03
Route TOPICAL
Dosage form CREAM
Substance OCTOCRYLENE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 87094-111-12 — 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 → 87094-0111-12. 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

LabelerBy the Beach Suncare LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87094
First marketedOct 2025
Product typeHuman Otc Drug
Portfolio8 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?

By the Beach Suncare SPF 30 is a topical cream sunscreen marketed as an over-the-counter monograph product. It contains three active ingredients: avobenzone, octisalate, and octocrylene, which are all ultraviolet (UV) filters commonly used in sunscreen formulations to help protect skin from sun exposure. These ingredients work together to absorb and scatter UV rays from the sun. The product is presented as a cream with a citrus crush scent.

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 E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • 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 H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII MCU2324216
    A silicone-based oil that reduces foaming and helps ingredients mix evenly. It's used as an antifoaming agent and lubricant in tablets, capsules, and liquid formulations.
  • UNII OSA9UP217S
    Dimethiconol is a silicone-based lubricant and anti-foaming agent. It reduces friction between tablet components and prevents foam formation during manufacturing and storage.
  • UNII 22ADO53M6F
    A mineral salt derived from phosphoric acid, used as a buffer to maintain the pH balance of the medication and help stabilize the active ingredients.
  • UNII 5QUO05548Z
    Palm oil is a natural plant-based fat extracted from palm fruit. It's used as a lubricant, binder, or coating agent to help the medicine hold together, flow smoothly during manufacturing, and sometimes improve how the body absorbs the active ingredient.
  • 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 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • UNII Z95S6G8201
    A synthetic surfactant derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oily and watery ingredients in liquid formulations, and may improve how the medicine spreads or is absorbed.
  • UNII D703131383
    Laponite is a synthetic clay mineral used in medicines as a thickener and stabilizer. It helps create the right texture in liquids and suspensions while keeping ingredients evenly mixed throughout the product.
  • 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 E2KR9C9V2I
    Polyacrylamide is a synthetic polymer used as a thickening agent and binder in medications. It helps create the proper texture and hold ingredients together in the formulation.
  • 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 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • 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 SE337SVY37
    A mineral salt used as a buffer to help maintain the medicine's pH level and prevent breakdown of active ingredients. It also acts as a thickening agent in liquid formulations.
  • 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 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 TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesAQUA, OCTOCRYLENE, ETHYLHEXYL SALICYLATE (OCTISALATE), PROPYLENE GLYCOL, ETHYLHEXYL PALMITATE, BUTYL METHOXYDIBENZOYLMETHANE (AVOBENZONE), GLYCERYL STEARATE, PEG-100 STEARATE, LITHIUM MAGNESIUM SILICATE, ELAEIS GUINEENSIS (PALM) OIL, PHENOXYETHANOL, STEARYL ALCOHOL, POLYACRYLAMIDE, FRAGRANCE, POTASSIUM CETYL PHOSPHATE, C13-14 ISOPARAFFIN, XANTHAN GUM, DIMETHICONE, CETYL ALCOHOL, LAURETH-7, ELAEIS GUINEENSIS (PALM) KERNEL OIL, ETHYLHEXYLGLYCERIN, HYDROXYETHYLCELLULOSE, DIMETHICONOL, CI 15985, CI 19140, DISODIUM PHOSPHATE, POLYSORBATE 60, SODIUM PHOSPHATE

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: 118 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
By the Beach Suncare 10 mg/100mL; 3 mg/100mL; 5 mg/100mLthis 87094-0111-12 By 177 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

🏛️
2025
On the market since
Oct 2025
📍
2026
Currently FDA-listed
1 year 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
87094-0111-11 118 mL in 1 TUBE (87094-111-11) 2025-10-03 Active
87094-0111-12 You're viewing this 177 mL in 1 TUBE (87094-111-12) 2025-10-03 Active

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

Pack size FAQ

What quantity is in NDC 87094-0111-12?
NDC 87094-0111-12 contains 177 mL — 177 ml in 1 tube.
What is the difference between NDC 87094-0111-12 and NDC 87094-0111-11?
Both are By the Beach Suncare SPF 30 Suncare Citrus Crush 10 mg/100mL; 3 mg/100mL; 5 mg/100mL Cream — the drug itself is identical. NDC 87094-0111-12 is the 177 mL package, while NDC 87094-0111-11 is the 118 ml package.
What NDC number is used to bill for this package of By the Beach Suncare SPF 30 Suncare Citrus Crush 10 mg/100mL; 3 mg/100mL; 5 mg/100mL Cream?
Bill NDC 87094-0111-12 — the 11-digit billing format is 87094011112. 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 87094-111-12, 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: 87094-0111-12, written without dashes as 87094011112. 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 87094-0111-12, the first segment (87094) is the labeler code FDA assigned to By the Beach Suncare LLC; the middle segment (0111) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (12) 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 By the Beach Suncare 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 118 ml (87094-0111-11). 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?
By the Beach Suncare 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 29 words ▾

Use Helps prevent sunburn If used with other sun protection measures (see below), helps to decrease the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 64 words ▾

Directions Shake well. Apply liberally and evenly 15 – 20 minutes before sun exposure Apply to all skin exposed to the sun Children under 6 months of age: Ask a doctor Re-apply immediately after spending time in the water Re-apply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating Warning: Reducing this quantity will lower the level of protection significantly

⚠️ Warnings 172 words ▾

Warnings Skin Cancer / Skin Aging Alert: Spending time in the sun increases your risk of skin cancer & early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Over-exposure to the sun is a serious health threat Do not use on damaged and/or broken skin When using this product keep out of eyes.

Rinse with water to remove. External use only. Stop use and ask a doctor if rash occurs Keep infants out of direct sunlight Do not stay too long in the sun, even while using a sunscreen product Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling 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. – 2 p.m. Wear long-sleeved shirts, pants, hats and sunglasses

📦 Storage and Handling 22 words ▾

Other information Protect the product in this container from excessive heat or direct sun This product helps with UVA & UVB protection

🧪 Active Ingredient 14 words ▾

Active Ingredient(s) Octocrylene (10%) – Sunscreen Octisalate (5%) – Sunscreen Avobenzone (3%) – Sunscreen

🧪 Inactive Ingredients 59 words ▾

Inactive ingredients AQUA, OCTOCRYLENE, ETHYLHEXYL SALICYLATE (OCTISALATE), PROPYLENE GLYCOL, ETHYLHEXYL PALMITATE, BUTYL METHOXYDIBENZOYLMETHANE (AVOBENZONE), GLYCERYL STEARATE, PEG-100 STEARATE, LITHIUM MAGNESIUM SILICATE, ELAEIS GUINEENSIS (PALM) OIL, PHENOXYETHANOL, STEARYL ALCOHOL, POLYACRYLAMIDE, FRAGRANCE, POTASSIUM CETYL PHOSPHATE, C13-14 ISOPARAFFIN, XANTHAN GUM, DIMETHICONE, CETYL ALCOHOL, LAURETH-7, ELAEIS GUINEENSIS (PALM) KERNEL OIL, ETHYLHEXYLGLYCERIN, HYDROXYETHYLCELLULOSE, DIMETHICONOL, CI 15985, CI 19140, DISODIUM PHOSPHATE, POLYSORBATE 60, SODIUM PHOSPHATE

🎯 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 ↗
← 87092-0004-02 · Guangzhou 87094-0112-11 · By →
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.