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Daily Facial Moisturizer SPF 25 Sunscreen .06 g/g; .03 g/g; .075 g/g; .015 g/g Cream, 45 g — NDC 00096-0721-45 package photo

Daily Facial Moisturizer SPF 25 Sunscreen .06 g/g; .03 g/g; .075 g/g; .015 g/g Cream, 45 g

by Person and Covey · 45 g in 1 BOTTLE (0096-0721-45)
NDC 00096-0721-45
🏷️ FDA NDC (as labeled) 0096-0721-45 billing pads the labeler segment with a zero
This package
Contains45 g Pack sizes2 compare ↓
Also comes in: 10 g 00096-0721-10
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 0096-0721-45
Product NDC 0096-0721
11-digit billing NDC 00096072145
NCPDP billing unit GM — per gram (weight)
UNII V06SV4M95S, G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM
Application # M020
SPL Set ID 6b9258e4-c7c6-765e-e053-2991aa0a9f4e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1991-08-01
Route TOPICAL
Dosage form CREAM
Substance HOMOSALATE; AVOBENZONE; OCTINOXATE; OCTOCRYLENE
GPI-14 90920000003700
GPI class DML Facial Moisturizer
GCN Seq No 016024
GCN 59620
HICL code 013205
Ingredient (HICL) Oxybenzone/Sunscreen/Hyalur Ac
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L2
Therapeutic class — intermediate (HIC2) Emollients
HIC3 code L2A
Therapeutic class — specific (HIC3) Emollients
AHFS code 84:24.12.00
AHFS class Basic Ointments And Protectants
FDB label name DML FACIAL MOISTURIZER CRM
FDB brand name Dml Facial Moisturizer
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 0096-0721-45 — 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 → 00096-0721-45. 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

LabelerPerson and Covey
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code00096
First marketedAug 1991
Product typeHuman Otc Drug
Portfolio23 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

Label name DML FACIAL MOISTURIZER CRM Ingredient Oxybenzone/Sunscreen/Hyalur Ac
🧪 What is this product?

This is a topical cream moisturizer labeled with sunscreen, marketed as an over-the-counter monograph product. It contains four active ingredients that function as ultraviolet (UV) filters, commonly used in sunscreens to help protect skin from sun exposure. Homosalate, avobenzone, octinoxate, and octocrylene are chemical sunscreen agents that absorb UV radiation. The product is intended for daily facial 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.

🧪 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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • 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 VT07D6X67O
    Cetyl phosphate is a waxy substance derived from fatty acids. It acts as an emulsifier to help mix oil and water-based ingredients, and may also serve as a thickener or stabilizer in creams and lotions.
  • 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 MCU2324216
    A silicone-based oil that reduces foaming and helps ingredients mix evenly. It's used as an antifoaming agent and lubricant in tablets, capsules, and liquid formulations.
  • UNII RGS4T2AS00
    A silicone-based lubricant and anti-foaming agent derived from silicon compounds. It reduces friction between tablet particles and equipment, helps prevent foam during manufacturing, and can be used as a coating agent in oral and topical products.
  • 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 RD25J5V947
    A waxy mixture derived from vegetable oils and polyethylene glycol that helps emulsify and blend oil-based and water-based ingredients. It's used in creams and lotions to create a smooth, uniform texture and improve product stability.
  • UNII SUS08ZOA9S
    A clay mineral used as a binder and anti-caking agent. It helps hold tablet ingredients together and prevents powders from clumping during storage.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 8D8I9Z0F1Z
    A synthetic oily liquid used as a solvent and plasticizer in medicines. It helps dissolve active ingredients and keeps coatings flexible in oral and topical formulations.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and 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 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 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII 035MV9S1C3
    A plastic-like polymer made from two chemical compounds joined together. It acts as a binder and film-former in tablets and capsules, helping hold ingredients together and create a protective coating on the medicine's surface.
  • 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.

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

The official label also statesPurified Water, Propylene Glycol Dioctanoate, Petrolatum, Glycerin, Glyceryl Stearate, PEG-100 Stearate, DEA-Cetyl Phosphate, Stearic Acid, Hyaluronic Acid, Benzyl Alcohol, Dimethicone, Cyclomethicone, PVP/Eicosene Copolymer, Silica, Sodium Carbomer 941, Allantoin, Disodium EDTA, Magnesium Aluminum Silicate

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: 10 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
Daily Facial Moisturizer SPF 25 .06 g/g; .03 g/g; .075 g/g; .015 g/gthis 00096-0721-45 Person 45 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

🏛️
1991
On the market since
Aug 1991
📍
2026
Currently FDA-listed
35 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
00096-0721-10 10 g in 1 TUBE (0096-0721-10) 2026-02-23 Active
00096-0721-45 You're viewing this 45 g in 1 BOTTLE (0096-0721-45) 1991-08-01 Active

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

Pack size FAQ

What quantity is in NDC 00096-0721-45?
NDC 00096-0721-45 contains 45 g — 45 g in 1 bottle.
What is the difference between NDC 00096-0721-45 and NDC 00096-0721-10?
Both are Daily Facial Moisturizer SPF 25 Sunscreen .06 g/g; .03 g/g; .075 g/g; .015 g/g Cream — the drug itself is identical. NDC 00096-0721-45 is the 45 g package, while NDC 00096-0721-10 is the 10 g package.
What NDC number is used to bill for this package of Daily Facial Moisturizer SPF 25 Sunscreen .06 g/g; .03 g/g; .075 g/g; .015 g/g Cream?
Bill NDC 00096-0721-45 — the 11-digit billing format is 00096072145. 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 0096-0721-45, 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: 00096-0721-45, written without dashes as 00096072145. 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 00096-0721-45, the first segment (00096) is the labeler code FDA assigned to Person and Covey; the middle segment (0721) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (45) 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 Person and Covey. 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 10 g (00096-0721-10). 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?
Person and Covey 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 18 words ▾

Uses -Moisturizes and helps to relieve irritated and sensitive skin -Higher SPF gives more sunburn protection -Water resistant

⏱️ Dosage and Administration 39 words ▾

Directions -Apply DML Daily Facial Moisturizer liberally and evenly 15-20 minutes before sun exposure and message in gently, allowing it to dry. Reapply as needed or as directed by your Dermatologist. -DML Daily Facial is an excellant make-up base.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 10 words ▾

Active Ingredients Octinoxate......7.5% Sunscreen Homosalate....6.0% Sunscreen Avobenzone...3.0% Sunscreen Octocrylene....1.5% Sunscreen

🧪 Inactive Ingredients 35 words ▾

Inactive Ingredients Purified Water, Propylene Glycol Dioctanoate, Petrolatum, Glycerin, Glyceryl Stearate, PEG-100 Stearate, DEA-Cetyl Phosphate, Stearic Acid, Hyaluronic Acid, Benzyl Alcohol, Dimethicone, Cyclomethicone, PVP/Eicosene Copolymer, Silica, Sodium Carbomer 941, Allantoin, Disodium EDTA, Magnesium Aluminum Silicate

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 00096-0709-35 · Person 00096-0732-04 · Person →
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.