Home › NDC Lookup › Ingredients › Zinc Oxide, Octinoxate, Oxybenzone, And... › 59555-0117-08
I.C. Industrial Sunscreen ZINC OXIDE, OCTINOXATE, OXYBENZONE, and OCTISALATE 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mL Lotion, 236 mL — NDC 59555-0117-08 package photo

I.C. Industrial Sunscreen ZINC OXIDE, OCTINOXATE, OXYBENZONE, and OCTISALATE 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mL Lotion, 236 mL

by R & R Lotion, Inc · 236 mL in 1 BOTTLE, DISPENSING (59555-117-08)
NDC 59555-0117-08
🏷️ FDA NDC (as labeled) 59555-117-08 billing pads the product segment with a zero
This package
Contains236 mL Pack sizes8 compare ↓
Also comes in: 4 ml 59555-0117-16 5 ml 59555-0117-01 50 ml 59555-0117-13 59 ml 59555-0117-04 118 ml 59555-0117-07 946 ml 59555-0117-10 3785 ml 59555-0117-11
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) 59555-117-08
Product NDC 59555-117
11-digit billing NDC 59555011708
UNII SOI2LOH54Z, 4Y5P7MUD51, 95OOS7VE0Y, 4X49Y0596W
Application # M020
SPL Set ID b89d687a-7b36-4643-9817-765d4710ca60
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-05-26
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE; OCTINOXATE; OXYBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 59555-117-08 — 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 → 59555-0117-08. 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.

🏭 Manufacturer & labeler

LabelerR & R Lotion, Inc
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code59555
First marketedMay 2022
Product typeHuman Otc Drug
Portfolio13 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 an over-the-counter lotion applied to the skin that contains four active ingredients commonly used as ultraviolet (UV) light filters in sunscreen products. Zinc oxide, octinoxate, octisalate, and oxybenzone are mineral and chemical UV absorbers typically used to help protect skin from sun exposure. This product is marketed under FDA's monograph rules for sunscreen lotions rather than as an individually approved drug application.

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

Color White
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 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 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII MBY1SL921L
    A plasticizer (softening agent) derived from organic compounds. It's added to tablet coatings and capsules to improve flexibility and prevent cracking during manufacturing and storage.
  • 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 EG3PA2K3K5
    Ethylhexyl stearate is a waxy oil made from stearic acid and ethylhexyl alcohol. In medicines, it acts as an emollient and thickener to improve texture and help the product spread smoothly on skin or dissolve properly.
  • 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 M629807ATL
    Imidazolidinyl urea is a synthetic preservative that prevents microbial growth in medicines. It's used in formulations to extend shelf life and maintain product safety during storage.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII 8Q0Z18J1VL
    A surfactant derived from oleic acid, a naturally occurring fatty acid. It helps mix oil and water-based ingredients together in formulations, improving product stability and texture.
  • 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 YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • 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 Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • 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.

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

The official label also statesDI Water, Ethylhexyl Stearate/Ethylhexyl Palmitate/Diethylhexy Adipate, Propylene Glycol, Glyceryl Stearate (and) PEG-100 Stearate, Cetearyl Alcohol (and) Cetearth-20 Xanthan Gum, Imidazolidinyl Urea, Methyl Paraben, Propyl Paraben, Oleth 3 Phosphate, Vitamin E

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: 4 ml 5 ml 50 ml 59 ml 118 ml 946 ml 3785 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
I.C. Industrial Sunscreen 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mLthis 59555-0117-08 R 236 ml — — FDA listed —
Beach Club Mineral Sunscreen 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mL 59555-0109-10 R 946 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

🏛️
2022
On the market since
May 2022
📍
2026
Currently FDA-listed
4 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
59555-0117-01 5 mL in 1 PACKET (59555-117-01) 2022-05-26 Active
59555-0117-04 59 mL in 1 BOTTLE, DISPENSING (59555-117-04) 2022-05-26 Active
59555-0117-07 118 mL in 1 BOTTLE, DISPENSING (59555-117-07) 2022-05-26 Active
59555-0117-08 You're viewing this 236 mL in 1 BOTTLE, DISPENSING (59555-117-08) 2022-05-26 Active
59555-0117-10 946 mL in 1 BOTTLE, PUMP (59555-117-10) 2022-05-26 Active
59555-0117-11 3785 mL in 1 BOTTLE, PUMP (59555-117-11) 2022-05-26 Active
59555-0117-13 50 mL in 1 BOTTLE, PUMP (59555-117-13) 2022-05-26 Active
59555-0117-16 4 mL in 1 PACKET (59555-117-16) 2022-05-26 Active

You're viewing one of 8 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 59555-0117-08?
NDC 59555-0117-08 contains 236 mL — 236 ml in 1 bottle, dispensing.
What is the difference between NDC 59555-0117-08 and NDC 59555-0117-16?
Both are I.C. Industrial Sunscreen ZINC OXIDE, OCTINOXATE, OXYBENZONE, and OCTISALATE 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mL Lotion — the drug itself is identical. NDC 59555-0117-08 is the 236 mL package, while NDC 59555-0117-16 is the 4 ml package.
What NDC number is used to bill for this package of I.C. Industrial Sunscreen ZINC OXIDE, OCTINOXATE, OXYBENZONE, and OCTISALATE 67.3 mg/mL; 57.5 mg/mL; 45 mg/mL; 38.3 mg/mL Lotion?
Bill NDC 59555-0117-08 — the 11-digit billing format is 59555011708. 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 59555-117-08, 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: 59555-0117-08, written without dashes as 59555011708. 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 59555-0117-08, the first segment (59555) is the labeler code FDA assigned to R & R Lotion, Inc; the middle segment (0117) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (08) 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 R & R Lotion, 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 7 other package presentations of this same product, including 4 ml (59555-0117-16), 5 ml (59555-0117-01), 50 ml (59555-0117-13). 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?
R & R Lotion, 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.
🎯 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 & early skin aging caused by the sun

⏱️ Dosage and Administration 86 words ▾

Directions apply liberally 15 minutes before sun exposure reapply: after 80 minutes of swimming or sweating immediately after towel drying every 2 hours 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 10am-2pm wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months: Ask a doctor

⚠️ Warnings 57 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 a rash occurs Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 11 words ▾

Other Information protect this product from excessive heat and direct sun

🧪 Active Ingredient 16 words ▾

Active Ingredients Purpose Zinc Oxide 6.73% Sunscreen Octinoxate 5.75% Sunscreen Benzophenone-3 4.50% Sunscreen Octisalate 3.83% Sunscreen

🧪 Inactive Ingredients 32 words ▾

Inactive Ingredients DI Water, Ethylhexyl Stearate/Ethylhexyl Palmitate/Diethylhexy Adipate, Propylene Glycol, Glyceryl Stearate (and) PEG-100 Stearate, Cetearyl Alcohol (and) Cetearth-20 Xanthan Gum, Imidazolidinyl Urea, Methyl Paraben, Propyl Paraben, Oleth 3 Phosphate, Vitamin E

🎯 Purpose 16 words ▾

Active Ingredients Purpose Zinc Oxide 6.73% Sunscreen Octinoxate 5.75% Sunscreen Benzophenone-3 4.50% Sunscreen Octisalate 3.83% Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 59555-0109-10 · R 59555-0200-01 · R →
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.