Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen Zinc Oxide and Octinoxate 120 mg/g; 75 mg/g Lotion, 1 tube — NDC 0023-5738-18 (Billing 00023-5738-18)
by Allergan, Inc. · 1 TUBE in 1 CARTON / 52.5 g in 1 TUBE
This is a package of 1 tube of Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen Zinc Oxide and Octinoxate 120 mg/g; 75 mg/g Lotion from Allergan, Inc., marketed since Mar 2016 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.
NDC 00023-5738-18
🏷️ FDA NDC (as labeled)
0023-5738-18
billing pads the labeler segment with a zero
This package
Contains1 tube
Pack sizes2 compare ↓
Main listing for product 0023-5738 · Also comes in:
6 tubes 0023-5738-25
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
NDC database record
One package, one record: these facts belong to NDC 0023-5738-18 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 0023 labeler · 5738 product · 18 package
- Package marketed since
- Mar 16, 2016
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 0023573818 2
- FDA record last changed
- Aug 27, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
0023-5738-18
Product NDC
0023-5738
11-digit billing NDC
00023573818
UNII
SOI2LOH54Z, 4Y5P7MUD51
Application #
M020
SPL Set ID
bc872876-20e7-40cb-b79d-68998883681a
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2016-03-16
Route
TOPICAL
Dosage form
LOTION
Substance
ZINC OXIDE; OCTINOXATE
Why two NDCs?
The FDA registers this code as 0023-5738-18 — a 4-4-2 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 labeler segment → 00023-5738-18. 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
🧪 What is this product?
This is a topical lotion labeled as an over-the-counter sunscreen, marketed under FDA's monograph rules for OTC skin protectants and sunscreens rather than through an individual drug approval. Its two active ingredients, zinc oxide and octinoxate, both function as UV filters that are typically used to help shield the skin from sunburn-causing ultraviolet radiation. Zinc oxide works as a mineral filter that sits on the skin's surface and scatters or reflects UV light, while octinoxate is an organic filter that absorbs UVB rays.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
💬 Questions about Zinc Oxide and Octinoxate?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per g | Per 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:
6 tubes
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 9, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 00023-5738-18 You're viewing this Main listing | 1 TUBE in 1 CARTON / 52.5 g in 1 TUBE | 2016-03-16 | — | Active |
| 00023-5738-25 0023-5738-25 | 6 TUBE in 1 CARTON / 7.1 g in 1 TUBE | 2016-03-16 | — | Active |
Pack size FAQ
What quantity is in this package?
This package contains 1 tube — 1 tube in 1 carton / 52.5 g in 1 tube.
How does this package differ from NDC 00023-5738-25?
Both are Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen Zinc Oxide and Octinoxate 120 mg/g; 75 mg/g Lotion — the drug itself is identical. This page's package is the 1 tube one, while NDC 00023-5738-25 is the 6 tubes package.
What NDC number is used to bill for this package of Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen Zinc Oxide and Octinoxate 120 mg/g; 75 mg/g Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen 120 mg/g; 75 mg/gthis 00023-5738-18 | Allergan, | 1 tube | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 9, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2016
On the market since
Mar 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.
- FDA Orange Book · refreshed Oct 9, 2026
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 A7E6112E4N
A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
-
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 00YIU5438U
Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
-
UNII 2968PHW8QP
A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
-
UNII 0THT5PCI0R
A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
-
UNII 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 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 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 W2ZU1RY8B0
A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
-
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 25X51I8RD4
Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
-
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 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 MVJ3AD73GG
A synthetic liquid derived from coconut oil and polyethylene glycol, used as an emulsifier and solubilizer to help mix water and oil-based ingredients and improve how the medicine dissolves and spreads throughout the formulation.
-
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 RLA2U05Z4Q
A silicone-based compound that acts as an emulsifier and skin-conditioning agent in topical formulations. It helps blend oil and water components together and creates a smooth, protective texture on the skin's surface.
-
UNII ZCD6009IUF
A plant-derived ingredient from knotweed used as a natural filler and binding agent. It helps hold the medicine's ingredients together and add bulk to tablets or capsules.
-
UNII 241BN7J12Y
Polyisobutylene is a synthetic rubber polymer used as a glidant and lubricant in tablets and capsules. It helps ingredients flow smoothly during manufacturing and reduces friction between particles.
-
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 X045WJ989B
Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
-
UNII LDC331P08E
A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
-
UNII X75PL53TZJ
A silicone-based polymer that functions as a glidant and anti-caking agent, helping the medicine powder flow smoothly during manufacturing and preventing clumping in the final product.
-
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.
24 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, Cyclopentasiloxane, Niacinamide, Oleth-3 Phosphate, Octyldodecyl Neopentanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Camellia Sinensis Leaf Extract, Polygonum Aviculare Extract, Tocopheryl Acetate, Sodium Hyaluronate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Triethoxycaprylylsilane, Polyisobutene, PEG-7 Trimethylolpropane Coconut Ether, Butylene Glycol, Disodium EDTA, Sodium Hydroxide, Citric Acid, Caprylyl Glycol, Sorbic Acid, Phenoxyethanol, Ethylhexylglycerin
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
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
LabelerAllergan, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code00023
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio188 products on file
More NDCs from Allergan, Inc. labeler code 00023
- Restasis MultiDose cyclosporine .5 mg/mL Emulsion NDC 0023-5301-05
- REFRESH OPTIVE Drops carboxymethylcellulose sodium and glycerin 10 mg/mL; 9 mg/mL Solution/ Drops NDC 0023-5459-02
- TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen Octinoxate, Octisalate and Zinc Oxide 75 mg/g; 30 mg/g; 80 mg/g Lotion NDC 0023-5494-01
- TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) Octinoxate, Octisalate, Titanium dioxide and Zinc Oxide 75 mg/g; 30 mg/g; 35 mg/g; 80 mg/g Lotion NDC 0023-5497-01
- Essential Defense Mineral Shield Broad Spectrum SPF 32 Sunscreen TINTED Titanium Dioxide and Zinc Oxide 50 mg/g; 60 mg/g Lotion NDC 0023-5675-08
- Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen Titanium Dioxide and Zinc oxide 50 mg/g; 60 mg/g Lotion NDC 0023-5703-08
- REFRESH Optive Mega-3 Carboxymethylcellulose sodium, Glycerin and Polysorbate 80 5 mg/mL; 10 mg/mL; 80 5 mg/mL Solution/ Drops NDC 0023-5773-05
- LILETTA Levonorgestrel 52 mg Intrauterine Device NDC 0023-5858-01
- Taytulla norethindrone acetate and ethinyl estradiol, and ferrous fumarate Kit NDC 0023-5862-29
- INFeD Iron Dextran 50 mg/mL Injection NDC 0023-6082-10
- Condylox podofilox 5 mg/g Gel NDC 0023-6118-03
- Crinone progesterone 45 mg/1.125g Gel NDC 0023-6150-04
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 openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
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
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Other Information
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses Helps prevent sunburn If used as directed with other sun protection measures (see Directions ) decreases the risk of skin cancer and early skin aging caused by the sun
⏱️ Dosage and Administration ▾
Directions Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hours Sun Protection Measures Spending time in the sun increases the risk of skin cancer, premature skin aging and other skin damage. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including limiting time in the sun from 10 a.m.-2 p.m., and wearing protective clothing Children under 6 months: Ask a doctor
⚠️ Warnings ▾
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 skin rash occurs Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredients Octinoxate 7.5% Zinc Oxide 12.0%
🧪 Inactive Ingredients ▾
Inactive ingredients Water, Cyclopentasiloxane, Niacinamide, Oleth-3 Phosphate, Octyldodecyl Neopentanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Camellia Sinensis Leaf Extract, Polygonum Aviculare Extract, Tocopheryl Acetate, Sodium Hyaluronate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Triethoxycaprylylsilane, Polyisobutene, PEG-7 Trimethylolpropane Coconut Ether, Butylene Glycol, Disodium EDTA, Sodium Hydroxide, Citric Acid, Caprylyl Glycol, Sorbic Acid, Phenoxyethanol, Ethylhexylglycerin
🎯 Purpose ▾
Purpose Sunscreen Sunscreen
📄 Do Not Use ▾
Do not use on damaged or broken skin
📄 When Using This Product ▾
When using this product keep out of eyes. Rinse with water to remove.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if skin rash occurs
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
📄 Other Information ▾
Other information Protect this product from excessive heat and direct sun Store at room temperature 15° - 30°C (59° - 86°F)
📄 Questions or Comments ▾
Questions or comments? www.skinmedica.com
📄 Package Label / Principal Display Panel ▾
Principal Display Panel - Carton Label Skin Medica ® ESSENTIAL DEFENSE EVERYDAY CLEAR™ BROAD SPECTRUM SPF 47 SUNSCREEN OILY & COMBINATION SKIN SUN PROTECTION Net Wt.
1.85Oz. / 52.5 g SkinMedica® ESSENTIAL DEFENSE EVERYDAY CLEAR™ BROAD SPECTRUM SPF 47 SUNSCREEN OILY & COMBINATION SKIN SUN PROTECTION Net Wt.
1.85Oz. / 52.5 g
Principal Display Panel - Tube Label Skin Medica ® ESSENTIAL DEFENSE EVERYDAY CLEAR™ BROAD SPECTRUM SPF 47 SUNSCREEN OILY & COMBINATION SKIN SUN PROTECTION Net Wt.
1.85Oz. / 52.5 g SkinMedica® ESSENTIAL DEFENSE EVERYDAY CLEAR™ BROAD SPECTRUM SPF 47 SUNSCREEN OILY & COMBINATION SKIN SUN PROTECTION Net Wt.
1.85Oz. / 52.5 g
No label section mentions that — try another word, or open the full label on DailyMed below.
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 Allergan, 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 1 other package presentation of this same product, including 6 tubes (00023-5738-25). 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?
Allergan, 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.
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.