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Tiege Hanley AM Morning Facial Moisturizer with SPF 20 Avobenzene, octinoxate, octocrylene 25 mg/mL; 55 mg/mL; 20 mg/mL Lotion, 22 mL — NDC 71714-0001-22 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tiege Hanley AM Morning Facial Moisturizer with SPF 20 Avobenzene, octinoxate, octocrylene 25 mg/mL; 55 mg/mL; 20 mg/mL Lotion, 22 mL — NDC 71714-001-22 (Billing 71714-0001-22)

by TIEGE HANLEY, Inc · 22 mL in 1 TUBE

This is a package of 22 mL of Tiege Hanley AM Morning Facial Moisturizer with SPF 20 Avobenzene, octinoxate, octocrylene 25 mg/mL; 55 mg/mL; 20 mg/mL Lotion from TIEGE HANLEY, Inc, marketed since Sep 2017 and currently FDA-listed, this package's marketing is listed to end Dec 2026. It is the main listing for this product, which comes in 2 package sizes.

NDC 71714-0001-22
🏷️ FDA NDC (as labeled) 71714-001-22 billing pads the product segment with a zero
This package
Contains22 mL Pack sizes2 compare ↓
Main listing for product 71714-001 · Also comes in: 75 ml 71714-001-75
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

NDC database record

One package, one record: these facts belong to NDC 71714-001-22 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71714 labeler · 001 product · 22 package
Package marketed since
Sep 30, 2017
Package marketing ended
Dec 31, 2026
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 7171400122 6
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71714-001-22
Product NDC 71714-001
11-digit billing NDC 71714000122
UNII G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM
Application # M020
SPL Set ID 22086cd8-2126-120e-e063-6394a90a561e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-09-30
Marketing end 2026-12-31
Route TOPICAL
Dosage form LOTION
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 71714-001-22 — 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 → 71714-0001-22. 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?

Tiege Hanley AM Morning Facial Moisturizer with SPF 20 is a topical lotion marketed as an over-the-counter monograph product. It contains three active ingredients that function as ultraviolet light filters: avobenzone, octinoxate, and octocrylene. These ingredients are typically used together in sunscreen products to help protect skin from UV radiation exposure when applied to the face and neck.

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.
Try another pack size: 75 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
71714-0001-22 You're viewing this Main listing 22 mL in 1 TUBE 2017-09-30 Dec 31, 2026 Active
71714-0001-75 71714-001-75 75 mL in 1 TUBE 2017-09-30 Dec 31, 2026 Active

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

Pack size FAQ

What quantity is in this package?
This package contains 22 mL — 22 ml in 1 tube.
How does this package differ from NDC 71714-0001-75?
Both are Tiege Hanley AM Morning Facial Moisturizer with SPF 20 Avobenzene, octinoxate, octocrylene 25 mg/mL; 55 mg/mL; 20 mg/mL Lotion — the drug itself is identical. This page's package is the 22 mL one, while NDC 71714-0001-75 is the 75 ml package.
What NDC number is used to bill for this package of Tiege Hanley AM Morning Facial Moisturizer with SPF 20 Avobenzene, octinoxate, octocrylene 25 mg/mL; 55 mg/mL; 20 mg/mL 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tiege Hanley AM Morning Facial Moisturizer with SPF 20 25 mg/mL; 55 mg/mL; 20 mg/mLthis 71714-0001-22 TIEGE 22 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

🏛️
2017
On the market since
Sep 2017
📍
2026
Currently FDA-listed
9 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 2JDK5W22H4
    A silicone-based substance that reduces surface tension and helps distribute ingredients evenly throughout the formula. It serves as an emulsifier and anti-foaming agent in medications.
  • 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 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 4Q93RCW27E
    A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
  • 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 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • 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 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 9M44R3409A
    A modified corn starch where some starch molecules have hydroxypropyl groups attached. It's used as a binder and disintegrant to help hold tablet ingredients together and allow the tablet to break apart properly when swallowed.
  • UNII W60VYE24XC
    A synthetic oily compound used as an emollient and solvent in topical medicines. It helps soften the skin, improve product spreadability, and dissolve active ingredients for better absorption through the skin.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7DC28K241X
    Plantago major leaf is a plant-derived ingredient used as a natural binder and thickening agent. It helps hold tablet ingredients together and may improve the product's texture or consistency.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • 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 1DXE3F3OZX
    A synthetic polymer that forms a gel-like network. It absorbs and holds water, thickens the medicine, and helps keep ingredients evenly mixed throughout the formulation.
  • 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 VX3T5G31XA
    A waxy ester derived from fatty acids, used as a lubricant and glidant to help powder particles flow smoothly during tablet or capsule manufacturing and to prevent sticking to equipment.
  • 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.

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

The official label also statesWater Isodecyl Neopentanoate Cyclopentasiloxane Bis-PEG-12 Dimethicone Beeswax Glycerin Glyceryl Stearate PEG-100 Stearate Phenoxyethanol Hydroxypropyl Starch Phosphate C18-38 Alkyl Hydroxystearoyl Stearate Caprylyl Glycol Carbomer Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Isohexadecane Lavandula Angustifolia (Lavender) Oil Rosmarinus Officinalis (Rosemary) Leaf Oil Sodium Hydroxide Polysorbate 80 Calendula Officinalis Flower Extract Plantago Major Leaf Extract Disodium EDTA

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

LabelerTIEGE HANLEY, Inc
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code71714
First marketedSep 2017
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from TIEGE HANLEY, Inc labeler code 71714

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 5 words ▾

Uses ■ Helps prevent sunburn

⏱️ Dosage and Administration 59 words ▾

Directions ■ After washing your face, massage a pea-sized amount into entire face and neck in a gentle circular motion ■ Before sun exposure, use a broad-spectrum sunscreen of SPF 15 or higher ■ Reapply sunscreen at least every two hours ■ Use a water-resistant sunscreen if swimming or sweating ■ For children under 6 months, ask a doctor

⚠️ Warnings 61 words ▾

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

🧪 Active Ingredient 8 words ▾

Active Ingredients Avobenzene 2.5% Octinoxate 5.5% Octocrylene 2.0%

🧪 Inactive Ingredients 52 words ▾

Water Isodecyl Neopentanoate Cyclopentasiloxane Bis-PEG-12 Dimethicone Beeswax Glycerin Glyceryl Stearate PEG-100 Stearate Phenoxyethanol Hydroxypropyl Starch Phosphate C18-38 Alkyl Hydroxystearoyl Stearate Caprylyl Glycol Carbomer Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Isohexadecane Lavandula Angustifolia (Lavender) Oil Rosmarinus Officinalis (Rosemary) Leaf Oil Sodium Hydroxide Polysorbate 80 Calendula Officinalis Flower Extract Plantago Major Leaf Extract Disodium EDTA

🎯 Purpose 1 words ▾

SUNSCREEN

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Package Label / Principal Display Panel 42 words ▾

Tiege Hanley AM Morning Facial Moisturizer with SPF 20 -

0.75FL. OZ. / 22mL Tiege Hanley AM Morning Facial Moisturizer

Tiege Hanley AM Morning Facial Moisturizer with SPF 20 -

2.5FL. OZ. / 75mL Tiege Hanley AM Morning Facial Moisturizer

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 it is currently marketed — but TIEGE HANLEY, Inc has reported a marketing end date of 2026-12-31, after which this package is expected to stop being marketed. 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 75 ml (71714-0001-75). 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?
TIEGE HANLEY, 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.
← 71713-0123-03 · THIRTY 71714-0003-24 · Tiege →
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.