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Double-Duty Face Moisturizer mositurizing sunscreen 2.2 g/1000g; 7.5 g/1000g Lotion, 251 g — NDC 66738-0020-19 package photo

Double-Duty Face Moisturizer mositurizing sunscreen 2.2 g/1000g; 7.5 g/1000g Lotion, 251 g

by Jack Black, LLC · 251 g in 1 BOTTLE (66738-020-19)
NDC 66738-0020-19
🏷️ FDA NDC (as labeled) 66738-020-19 billing pads the product segment with a zero
This package
Contains251 g Pack sizes7 compare ↓
Also comes in: 2 g 66738-0020-02 14 g 66738-0020-50 30 g 66738-0020-01 44 g 66738-0020-04 97 g 66738-0020-03 480 g 66738-0020-16
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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) 66738-020-19
Product NDC 66738-020
11-digit billing NDC 66738002019
UNII G63QQF2NOX, 4Y5P7MUD51
Application # M020
SPL Set ID 672be406-e3a1-47b4-8ef6-ee2b62baae96
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2009-05-29
Route TOPICAL
Dosage form LOTION
Substance AVOBENZONE; OCTINOXATE
Why two NDCs? The FDA registers this code as 66738-020-19 — 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 → 66738-0020-19. 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

LabelerJack Black, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code66738
First marketedMay 2009
Product typeHuman Otc Drug
Portfolio17 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 lotion marketed as an over-the-counter monograph product under FDA's established rule-book for sunscreens and skin-care products. It contains avobenzone and octinoxate, which are ultraviolet light absorbers commonly used in sunscreen formulations to help protect skin from UVA and UVB radiation. The product is also formulated with moisturizing ingredients intended to hydrate the skin. As an OTC monograph drug, it is manufactured under FDA guidelines for this category rather than through an individual product 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 9NT987I3A8
    A natural oil derived from apple fruit, used as a flavoring agent and fragrance component to add apple taste and aroma to the medicine.
  • UNII 91OLL9AJ7D
    A plant extract from Artemisia umbelliformis flowers, used as a flavoring agent or botanical ingredient to add taste or aroma to the medicine.
  • UNII X380815D32
    A plant extract from butterfly bush leaves used as a natural colorant and flavoring agent in medicines. It may also help preserve the product or provide antioxidant properties in the formulation.
  • 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 P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII Z135WT9208
    Carbomer is a synthetic polymer that forms a thick, gel-like consistency. It's used in medicines as a thickener and stabilizer to improve texture and keep ingredients evenly mixed throughout the product.
  • UNII F68VH75CJC
    A synthetic polymer made from acrylic acid that thickens and stabilizes liquid or gel formulations. It's used as a gelling agent and emulsifier to create the desired texture and consistency in topical medicines.
  • UNII 09FUA47KNA
    Cetearyl glucoside is a plant-derived surfactant made from vegetable oils and glucose. It helps oils and water mix together in creams and lotions, and can also soften and smooth the skin feel of the product.
  • UNII UB27587839
    A plant-derived oil from Roman chamomile flowers. It's used in medicines as a flavoring agent and fragrance to improve taste and smell.
  • UNII NMQ347994Z
    Cyclomethicone is a silicone-based fluid that acts as a lubricant and solvent in medicines. It helps products flow smoothly, reduces friction between particles, and aids in even distribution of active ingredients.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 7832HOY4ZQ
    A red seaweed extract used as a thickener and stabilizer in liquid medicines and suspensions. It helps maintain consistent texture and keeps ingredients evenly mixed throughout the product.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII NNE56F2N14
    A synthetic compound derived from glycerin and polyethylene glycol. It acts as an emulsifier and solubilizer to help mix water and oil-based ingredients and keep them blended throughout the product's shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII Y87200QHN9
    A natural brownish pigment derived from a marine diatom (single-celled algae), used as a colorant to tint the medicine brown or provide visual identification.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 86FQE96TZ4
    A synthetic polymer, this ingredient acts as a thickener and suspending agent in liquid formulations. It helps maintain uniform consistency and keeps particles evenly distributed throughout the medicine.
  • UNII 603P14DHEB
    A synthetic antimicrobial chemical used as a preservative in topical and cosmetic formulations. It prevents bacterial and fungal growth in products to maintain stability and safety during storage and use.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • 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 MWN6IZU3XM
    A plant extract from edelweiss flowers. It's used in medicines as a natural ingredient to help preserve the product and may contribute to texture or appearance.
  • UNII PTP6R7263M
    A plant-derived oil extracted from melissa (lemon balm) leaves. Used as a flavoring agent and fragrance to improve the taste or smell of the medicine.
  • UNII X8725R883T
    A synthetic oily liquid derived from branched carboxylic acids, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII 3K0J1S7QGC
    A fragrant essential oil derived from geranium flowers, used as a flavoring and fragrance agent to improve the taste and aroma of medicines.
  • UNII 86P27YRR6Y
    A plant extract from peucedanum ostruthium leaves used as a natural flavoring or aromatic ingredient in medicines. It may help provide taste or scent to make the medication more palatable.
  • UNII 0C143929GK
    Phenethyl benzoate is a synthetic fragrance and flavoring agent used in medicines to mask unpleasant tastes or add pleasant aroma to improve patient acceptance of the medication.
  • 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 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • 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 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.

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

The official label also statesPurified Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenylethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate / Sodium Acryloyl Dimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavendula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens (Geranium) Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis (Balm Mint) Extract, Haslea Ostreaia (Blue Algae) Extract, Palmaria Palmata (Sea Parsley) Extract, Calendula Officinalis (Calendula) Flower Extract, Glycerin, Leontopodium Alöinum (Edelweiss) Extract, Artemisia Umbelliformis Extract, Buddleja Davidii Leaf Extract, Peucedanum Ostruthium Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Anthemis Nobilis (Roman Chamomile) Flower 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 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: 2 g 14 g 30 g 44 g 97 g 480 g
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
Double-Duty Face Moisturizer 2.2 g/1000g; 7.5 g/1000gthis 66738-0020-19 Jack 251 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

🏛️
2009
On the market since
May 2009
📍
2026
Currently FDA-listed
17 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
66738-0020-01 30 g in 1 TUBE (66738-020-01) 2020-04-01 Active
66738-0020-02 2 g in 1 PACKET (66738-020-02) 2020-03-11 Active
66738-0020-03 97 g in 1 BOTTLE (66738-020-03) 2009-05-29 Active
66738-0020-04 44 g in 1 TUBE (66738-020-04) 2009-07-30 Active
66738-0020-16 480 g in 1 BOTTLE (66738-020-16) 2020-05-01 Active
66738-0020-19 You're viewing this 251 g in 1 BOTTLE (66738-020-19) 2011-06-15 Active
66738-0020-50 14 g in 1 TUBE (66738-020-50) 2020-03-11 Active

You're viewing one of 7 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 66738-0020-19?
NDC 66738-0020-19 contains 251 g — 251 g in 1 bottle.
What is the difference between NDC 66738-0020-19 and NDC 66738-0020-02?
Both are Double-Duty Face Moisturizer mositurizing sunscreen 2.2 g/1000g; 7.5 g/1000g Lotion — the drug itself is identical. NDC 66738-0020-19 is the 251 g package, while NDC 66738-0020-02 is the 2 g package.
What NDC number is used to bill for this package of Double-Duty Face Moisturizer mositurizing sunscreen 2.2 g/1000g; 7.5 g/1000g Lotion?
Bill NDC 66738-0020-19 — the 11-digit billing format is 66738002019. 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 66738-020-19, 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: 66738-0020-19, written without dashes as 66738002019. 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 66738-0020-19, the first segment (66738) is the labeler code FDA assigned to Jack Black, LLC; the middle segment (0020) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (19) 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 Jack Black, 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 6 other package presentations of this same product, including 2 g (66738-0020-02), 14 g (66738-0020-50), 30 g (66738-0020-01). 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?
Jack Black, 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 4 words ▾

Use Helps prevent sunburn

⏱️ Dosage and Administration 81 words ▾

Directions Apply liberally 15 minutes before sun exposure Use a water resisitant sunscreen if swimming or sweating Reapply at least every two hours 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, use sunscreen with a broad spectrum SPF15 or higher Limit time in the sun, especxially from 10 a.m. - 2 p.m.

Wear long sleeve shirts, pants, hats and sunglasses.

⚠️ Warnings 52 words ▾

Warnings For external use only Do not use on damaged or broken skin Stop use and ask doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away

🧪 Active Ingredient 8 words ▾

Active Ingredients Avobenzone 2.2% Sunscreen Octinoxate 7.5% Sunscreen

🧪 Inactive Ingredients 102 words ▾

Inactive Ingredients Purified Water, Cyclopentasiloxane, Octyldodecyl Neopentanoate, Phenylethyl Benzoate, Dimethicone, Glycereth-26, Hydroxyethyl Acrylate / Sodium Acryloyl Dimethyl Taurate Copolymer, Phenoxyethanol, Hydroxypropyl Starch Phosphate, Cetearyl Glucoside, Carbomer, Pyrus Malus (Apple) Fruit Extract, Butylene Glycol, Sodium Hydroxide, Disodium EDTA, Sodium Hyaluronate, Lavendula Angustifolia (Lavender) Oil, Iodopropynyl Butylcarbamate, Pelargonium Graveolens (Geranium) Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lecithin, Melissa Officinalis (Balm Mint) Extract, Haslea Ostreaia (Blue Algae) Extract, Palmaria Palmata (Sea Parsley) Extract, Calendula Officinalis (Calendula) Flower Extract, Glycerin, Leontopodium Alöinum (Edelweiss) Extract, Artemisia Umbelliformis Extract, Buddleja Davidii Leaf Extract, Peucedanum Ostruthium Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Anthemis Nobilis (Roman Chamomile) Flower Oil

🎯 Purpose 4 words ▾

Use Helps prevent sunburn

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 66733-0958-23 · ImClone 66738-0022-01 · Jack →
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.