Home › NDC Lookup › Ingredients › Meradimate, Octinoxate, Oxybenzone, And... › 70605-0014-21
Principal Secret Reclaim Sunscreen For Face and Body SPF 30 Meradimate, Octinoxate, Oxybenzone, and Zinc Oxide 3.5 mg/100mL; 7.5 mg/100mL; 2 mg/100mL; 3 mg/100mL Cream, 75 mL — NDC 70605-0014-21 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Principal Secret Reclaim Sunscreen For Face and Body SPF 30 Meradimate, Octinoxate, Oxybenzone, and Zinc Oxide 3.5 mg/100mL; 7.5 mg/100mL; 2 mg/100mL; 3 mg/100mL Cream, 75 mL — NDC 70605-014-21 (Billing 70605-0014-21)

by Guthy-Renker LLC · 75 mL in 1 TUBE

This is a package of 75 mL of Principal Secret Reclaim Sunscreen For Face and Body SPF 30 Meradimate, Octinoxate, Oxybenzone, and Zinc Oxide 3.5 mg/100mL; 7.5 mg/100mL; 2 mg/100mL; 3 mg/100mL Cream from Guthy-Renker LLC, marketed since Apr 2016 and currently FDA-listed. It is this product's only package size.

NDC 70605-0014-21
🏷️ FDA NDC (as labeled) 70605-014-21 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70605-014-21
Product NDC 70605-014
11-digit billing NDC 70605001421
UNII J9QGD60OUZ, 4Y5P7MUD51, 95OOS7VE0Y, SOI2LOH54Z
Application # M020
SPL Set ID 4a183aa2-deda-4b26-a126-6f98cfbdb0f3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-04-30
Route TOPICAL
Dosage form CREAM
Substance MERADIMATE; OCTINOXATE; OXYBENZONE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 70605-014-21 — 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 → 70605-0014-21. 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?

Principal Secret Reclaim Sunscreen For Face and Body is a topical cream containing four active ingredients that function as ultraviolet (UV) filters. Meradimate, octinoxate, and oxybenzone are chemical sunscreen agents that absorb UV radiation, while zinc oxide is a mineral sunscreen agent that reflects UV light. This product is marketed as an over-the-counter monograph sunscreen and is typically used to help protect skin from sun exposure when applied to the face and body.

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.
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
70605-0014-21 You're viewing this Main listing 75 mL in 1 TUBE 2017-11-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Principal Secret Reclaim Sunscreen For Face and Body SPF 30 3.5 mg/100mL; 7.5 mg/100mL; 2 mg/100mL; 3 mg/100mLthis 70605-0014-21 Guthy-Renker 75 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
Apr 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.

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 UN2QZ55I88
    A plant-derived ingredient from abelmoschus moschatus seeds. It's used in formulations as a thickening agent, emulsifier, and texture enhancer to help bind and stabilize medicine ingredients.
  • UNII L4EL31FWIL
    A synthetic peptide (short chain of amino acids) used as a conditioning or texture-enhancing agent in topical formulations. It helps improve product feel and skin compatibility in creams and lotions.
  • UNII SMF2K46G8D
    A red algae extract used as a gelling agent and thickener in medicines. It forms a gel-like consistency that helps control how the medicine releases and is absorbed in the body.
  • UNII QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 4AJZ4765R9
    A flavoring agent derived from bananas that gives medicine a banana taste. It's added to make oral medications more palatable, especially for children.
  • UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • 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 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 I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • UNII 430RJA6715
    A synthetic oily liquid used in topical formulations as an emollient and penetration enhancer. It helps soften the skin and allows active ingredients to absorb more effectively through the skin.
  • 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 YCZ8EM144Q
    A fat derived from palm oil that has been chemically treated to make it more stable. It acts as a binder and lubricant in tablets and capsules, helping hold ingredients together and prevent sticking during manufacturing.
  • UNII M30XO5X4XD
    A dried plant root extract from Florentine iris used as a natural fragrance, flavoring, and binding agent in medications. It helps hold tablet ingredients together and adds mild pleasant taste or aroma.
  • 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 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • 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 ZV095H5633
    A natural flavoring derived from muskmelon fruit. It is used in medicines to add pleasant taste and aroma, making the product more acceptable to take.
  • UNII 19F5HK2737
    Pantothenic acid is a B vitamin used in some formulations as a nutritional supplement or to support stability. It may also serve as a buffer or pH adjuster in the medicine.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • 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 A034SE7857
    Phytonadione is a form of vitamin K, a naturally occurring compound. It's used in medicines as an active pharmaceutical ingredient to support blood clotting, though it may also serve as a colorant or stabilizer in some formulations.
  • 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 ZI1LK470XV
    A synthetic emulsifier made from glycerin and stearic acid. It helps keep oil and water mixed together in the product and improves texture and stability.
  • 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 YWI33EV595
    A synthetic compound derived from a fatty alcohol, used as an emulsifier and surfactant to help mix oil and water components in medicines, and to improve how the product spreads or flows.
  • UNII XF4K22WN6T
    A synthetic oil derived from glycerin and branched fatty acids. It acts as a solvent and lubricant in medications, helping dissolve active ingredients and improve how the medicine flows and spreads.
  • 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 R1H893D80E
    A plant extract from grapevine leaves used as a natural colorant and antioxidant in medications. It helps preserve the medicine's stability and may contribute to the product's color.
  • 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.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesWater, Ethylhexyl Ethylhexanoate, Pentylene Glycol, Triisononanoin, Sodium Dihydroxycetyl Phosphate, Glyceryl Stearate SE, Cetearyl Alcohol, Beeswax, Glycosaminoglycans, Ahnfeltiopsis Concinna Extract, Acetyl Hexapeptide-8, Phospholipids, Tocopheryl Acetate, Retinyl Palmitate, Cucumis Melo (Melon) Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Ascorbyl Palmitate, Pantothenic Acid, Vitis Vinifera (Grape) Leaf Extract, Iris Florentina Root Extract, Hibiscus Abelmoschus Extract, Bisabolol, Hydrogenated Palm Glycerides, Ceteareth-20, Polyglyceryl-3 Caprate, Phytonadione, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Xanthan Gum, Caprylic/Capric Triglyceride, Butylene Glycol, Phenoxyethanol, Methylparaben, Chlorphenesin, Benzoic Acid

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

LabelerGuthy-Renker LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code70605
First marketedApr 2016
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.

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 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 4 words ▾

Uses helps prevent sunburn

⏱️ Dosage and Administration 30 words ▾

Directions apply liberally 15 minutes before sub exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months Ask a doctor.

⚠️ Warnings 91 words ▾

Warnings Skin Cancer/Skin Aging Alert Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging. 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.

📦 Storage and Handling 11 words ▾

Other Information protect this product from excessive heat and direct sun

🧪 Active Ingredient 11 words ▾

Active ingredient Octinoxate 7.5% Meradimate 3.5% Zinc Oxide 2.0% Oxybenzone 2.0%

🧪 Inactive Ingredients 77 words ▾

Inactive ingredients Water, Ethylhexyl Ethylhexanoate, Pentylene Glycol, Triisononanoin, Sodium Dihydroxycetyl Phosphate, Glyceryl Stearate SE, Cetearyl Alcohol, Beeswax, Glycosaminoglycans, Ahnfeltiopsis Concinna Extract, Acetyl Hexapeptide-8, Phospholipids, Tocopheryl Acetate, Retinyl Palmitate, Cucumis Melo (Melon) Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Ascorbyl Palmitate, Pantothenic Acid, Vitis Vinifera (Grape) Leaf Extract, Iris Florentina Root Extract, Hibiscus Abelmoschus Extract, Bisabolol, Hydrogenated Palm Glycerides, Ceteareth-20, Polyglyceryl-3 Caprate, Phytonadione, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Xanthan Gum, Caprylic/Capric Triglyceride, Butylene Glycol, Phenoxyethanol, Methylparaben, Chlorphenesin, Benzoic Acid

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 21 words ▾

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 9 words ▾

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Questions or Comments 4 words ▾

Questions or comments? 800-510-4961

📄 Package Label / Principal Display Panel 36 words ▾

PRINCIPAL DISPLAY PANEL - 75 mL Tube Label PRINCIPAL SECRET ® RECLAIM ® with Argireline ® Sunscreen For Face & Body SPF 30 75 mL

2.5FL. OZ. PRINCIPAL DISPLAY PANEL - 75 mL Tube Label

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

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 Guthy-Renker LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guthy-Renker 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.
← 70600-0084-01 · Maithri 70605-0017-34 · Guthy-Renker →
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.