HomeNDC LookupIngredientsTitanium Dioxide Zinc Oxide › 85591-0203-50
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(from DailyMed)

Tinted Mineral Primer SPF 40 Titanium Dioxide, Zinc Oxide 80 mg/g; 38 mg/g Cream, 53 g

by JOSEPHINA RAMIREZ · 53 g in 1 BOTTLE, PUMP (85591-203-50)
NDC 85591-0203-50
🏷️ FDA NDC (as labeled) 85591-203-50 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Titanium Dioxide, Zinc Oxide (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Sep 3, 2024 — Microbial Contamination of Non-Sterile Product (Vivier Pharma, Inc.) · FDA recall D-0662-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 85591-203-50
Product NDC 85591-203
11-digit billing NDC 85591020350
UNII 15FIX9V2JP, SOI2LOH54Z
Application # M020
SPL Set ID 365cf2be-8862-3622-e063-6394a90ac4e3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-04-16
Route TOPICAL
Dosage form CREAM
Substance TITANIUM DIOXIDE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 85591-203-50 — 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 → 85591-0203-50. 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

LabelerJOSEPHINA RAMIREZ
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code85591
First marketedApr 2021
Product typeHuman Otc Drug
Portfolio2 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 tinted mineral sunscreen cream applied to the skin, marketed as an over-the-counter product under FDA's sunscreen monograph rules. The active ingredients are titanium dioxide and zinc oxide, both mineral UV filters that work by sitting on top of the skin to reflect and scatter ultraviolet light. The product is formulated to provide sun protection (SPF 40) while also adding light color to the skin. It is a cosmetic sunscreen commonly used for daily facial protection.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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.
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
Priia Tinted Mineral Sunscreen and Primer 80 mg/g; 38 mg/g 81493-0203-50 Priia 53 g FDA listed
Shaded 80 mg/g; 38 mg/g 85319-0203-15 Potency 1.5 g FDA listed
Prime And Protect Matte 80 mg/g; 38 mg/g 85363-0203-50 Kalon 53 g FDA listed
non-tinted face mineral sunscreen SPF40 80 mg/g; 38 mg/g 85370-0202-50 Lisa 53 g FDA listed
Non-Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85376-0202-15 HSC 15 g FDA listed
Complexion Correction Tinted Primer Sunscreen 80 mg/g; 38 mg/g 85449-0201-85 MCRAE 85 g FDA listed
Tinted Primer Anti-Aging 80 mg/g; 38 mg/g 85466-0203-50 DERMOPERFECTION 53 g FDA listed
Tinted SPF40 80 mg/g; 38 mg/g 85531-0203-50 JOHANNA'S 53 g FDA listed
Mattifying Mineral SPF 40 Tinted 80 mg/g; 38 mg/g 85555-0201-85 ELIZA 85 g FDA listed
Tinted Mineral Primer SPF 40 80 mg/g; 38 mg/gthis 85591-0203-50 JOSEPHINA 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85597-0203-50 ESTHETIC 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85604-0203-15 ESTHETICS 15 g FDA listed
Advanced Sun Protection 80 mg/g; 38 mg/g 85609-0201-85 HELLO 85 g FDA listed
Prime Protection Sunscreen, tinted 80 mg/g; 38 mg/g 85641-0203-15 KRISTI 1.5 g FDA listed
Mattify Total Protection Sunscreen 80 mg/g; 38 mg/g 85752-0203-50 CLEAN 53 g FDA listed
PURE Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85774-0203-50 LA 53 g FDA listed
Scalp Sunscreen 80 mg/g; 38 mg/g 85846-0203-50 FOLICULE 53 g FDA listed
Mineral Sunscreen Tinted 80 mg/g; 38 mg/g 87003-0203-50 YUMA 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 87049-0203-50 THE 53 g FDA listed
Priia Tinted Mineral Sunscreen and Primer 80 mg/g; 38 mg/g 81493-0201-80 Priia 85 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85302-0203-50 Face 50 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85327-0203-50 Rhonda 53 g FDA listed
Tinted Mineral Matte CE Sunscreen 80 mg/g; 38 mg/g 85394-0203-50 The 53 g FDA listed
Mineral Fusion Tinted 80 mg/g; 38 mg/g 85416-0203-15 FOREFRONT 15 g FDA listed
SUNerchi Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85422-0203-50 SYNERCHI 53 g FDA listed
sheer tinted matte mineral 80 mg/g; 38 mg/g 85575-0203-50 NEXTEX 53 g FDA listed
Daily Defense Facial Sunscreen Plus Primer 80 mg/g; 38 mg/g 85596-0203-50 LAURA 53 g FDA listed
Happy Mineral Sunscreen Primer SPF 80 mg/g; 38 mg/g 85723-0203-50 ACNE 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85728-0203-50 Dermacare 53 g FDA listed
Sheer Mineral Sunscreen Silk Matte Finish 80 mg/g; 38 mg/g 85317-0202-50 TRU 53 g FDA listed
Smoothing Mineral Sunscreen Non-Tinted 80 mg/g; 38 mg/g 85328-0202-50 DANIEL 53 g FDA listed
Proper Protection Plus Primer Tinted 80 mg/g; 38 mg/g 85358-0203-50 Skin 53 g FDA listed
Mineral Sunscreen 80 mg/g; 38 mg/g 85382-0203-50 DAISY'S 53 g FDA listed
Sheer Mineral Sunscreen 80 mg/g; 38 mg/g 85394-0202-50 The 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85513-0203-50 THE 53 g FDA listed
Sun Elegant Mineral Sunscreen Tinted 80 mg/g; 38 mg/g 85519-0203-50 SKIN 53 g FDA listed
Facial Mineral Sunscreen Mineral Protection 80 mg/g; 38 mg/g 85627-0203-50 CAPE 53 g FDA listed
Tinted Facial Protection SPF40 80 mg/g; 38 mg/g 85630-0203-50 FRESH 53 g FDA listed
Day Defense Tinted 80 mg/g; 38 mg/g 85695-0203-50 THE 53 g FDA listed
Mineral Matte Non-Tinted Sunscreen 80 mg/g; 38 mg/g 85939-0202-50 ORAIOS 53 g FDA listed
PROCEUTICALS PRIVATE LABEL by TiZO tinted mineral sunscreen 80 mg/g; 38 mg/g 58892-0203-50 Fallien 53 g FDA listed
HUTTON KLEIN HK DERMATOLOGISTS SPF 40 Mineral Based Facial Sunscreen Tinted 80 mg/g; 38 mg/g 81679-0203-50 Hutton, 53 g FDA listed
Matte Mineral Sunscreen 80 mg/g; 38 mg/g 85330-0203-50 Skin 53 g FDA listed
Mineral Primer tinted SPF40 80 mg/g; 38 mg/g 85356-0203-50 Oracle 53 g FDA listed
Proper Protection Plus Primer NT 80 mg/g; 38 mg/g 85358-0202-15 Skin 1.5 g FDA listed
Tinted Mineral 40 80 mg/g; 38 mg/g 85392-0203-15 2301 1.5 g FDA listed
Replenishing Tinted Sunscreen 80 mg/g; 38 mg/g 85418-0203-50 Beauty 53 g FDA listed
Complexion Correction Primer Sunscreen clear 80 mg/g; 38 mg/g 85449-0202-15 MCRAE 1.5 g FDA listed
Complexion Correction Tinted Primer Sunscreen 80 mg/g; 38 mg/g 85449-0203-15 MCRAE 1.5 g FDA listed
Anti-Aging Sun Protection NT 80 mg/g; 38 mg/g 85466-0202-50 DERMOPERFECTION 53 g FDA listed
Skin Filter Matte SPF 80 mg/g; 38 mg/g 85496-0203-50 MALORIE 53 g FDA listed
Tinted Facial Mineral Sunscreen SPF 40 80 mg/g; 38 mg/g 85508-0203-15 RSL89 1.5 g FDA listed
Rejuvn8 80 mg/g; 38 mg/g 85635-0203-50 FLEUR 53 g FDA listed
Matte Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85642-0203-50 EDIT 53 g FDA listed
Tinted Facial Sunscreen 80 mg/g; 38 mg/g 85679-0203-50 HELTON 53 g FDA listed
Age Defying Mineral Protection 80 mg/g; 38 mg/g 85715-0202-50 MARK 53 g FDA listed
Non-Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 87049-0202-50 THE 53 g FDA listed
Perfect Mineral Sunscreen 80 mg/g; 38 mg/g 87162-0203-15 SKIN 1.5 g FDA listed
Anti-Aging Tinted Sunscreen 80 mg/g; 38 mg/g 87444-0201-85 LASER 85 g FDA listed
Shunly Radiant Translucent SPF 40 80 mg/g; 38 mg/g 81381-0202-50 Shunly 53 g FDA listed
Healthy Mineral Sunscreen No Shine - No Tint 80 mg/g; 38 mg/g 85338-0202-50 Zen 53 g FDA listed
Dr B Clinical Skin Care Non Tinted Sunscreen 80 mg/g; 38 mg/g 85365-0202-50 NAIRA 53 g FDA listed
Tinted Minerals 1point8 oz 80 mg/g; 38 mg/g 85395-0203-50 SPECKTRA6 53 g FDA listed
UV Defense Mineral Sunscreen 80 mg/g; 38 mg/g 85495-0202-50 CCLEAR 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85585-0203-50 JEFFREY 53 g FDA listed
Soft Focus Mineral Defense Tinted 80 mg/g; 38 mg/g 85607-0203-50 SPOTLESS 53 g FDA listed
Mineral Mousse 80 mg/g; 38 mg/g 85629-0203-50 CLARITY 53 g FDA listed
Facial Mineral Sunscreen Tinted 80 mg/g; 38 mg/g 85634-0203-50 DR. 53 g FDA listed
UV Protection Veil Mineral Sunscreen non tinted 80 mg/g; 38 mg/g 85926-0202-50 ATHENA 53 g FDA listed
sheer tinted sunscreen 80 mg/g; 38 mg/g 85968-0203-50 SARA 53 g FDA listed
CoTZ Face Prime and Protect SPF 40 (Tinted) 80 mg/g; 38 mg/g 58892-0354-45 Fallien 1 tube FDA listed
Shunly Radiant Translucent Tinted SPF 40 80 mg/g; 38 mg/g 81381-0203-50 Shunly 53 g FDA listed
BHSkin Sheer Tinted Zinc and Titanium SPF 40 80 mg/g; 38 mg/g 83095-0203-50 Don 53 g FDA listed
Silk Screen 80 mg/g; 38 mg/g 83628-0201-85 Skin 85 g FDA listed
Protect Mineral Sunscreen Non-Tinted 80 mg/g; 38 mg/g 85314-0202-50 Melinda 53 g FDA listed
Mineral Primer non-tinted SPF40 80 mg/g; 38 mg/g 85356-0202-50 Oracle 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85376-0203-50 HSC 53 g FDA listed
Tinted Mineral Moisturizing Sunscreen 80 mg/g; 38 mg/g 85490-0203-50 ABOUT 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85492-0203-50 The 53 g FDA listed
Facial Mineral Fusion 80 mg/g; 38 mg/g 85507-0203-50 IT 53 g FDA listed
Prime and Protect 80 mg/g; 38 mg/g 85557-0203-50 Shannon 53 g FDA listed
non-tinted sheer matte mineral 80 mg/g; 38 mg/g 85575-0202-50 NEXTEX 53 g FDA listed
Matte Finish 80 mg/g; 38 mg/g 85599-0203-15 CLEAN 1.5 g FDA listed
Tinted Primer Mineral Sunscreen 80 mg/g; 38 mg/g 85640-0203-50 CECILIA 53 g FDA listed
Barrier Plus Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85726-0203-50 Healthy 53 g FDA listed
Mineral Sunscreen Non Tinted 80 mg/g; 38 mg/g 85798-0202-50 SAN 53 g FDA listed
Mineral Sunscreen Tinted 80 mg/g; 38 mg/g 85987-0203-50 ESTHETICS 53 g FDA listed
Proceuticals Private Label by TiZO Tinted Facial Mineral Sunscreen Backbar 80 mg/g; 38 mg/g 58892-0201-85 Fallien 85 g FDA listed
Flawless Brightening Sunscreen 80 mg/g; 38 mg/g 81535-0201-85 Flawless 85 g FDA listed
Mineral SPF 40, Tinted 80 mg/g; 38 mg/g 85292-0203-15 Acne 1.5 g FDA listed
Tinted Physical Block Sunscreen 80 mg/g; 38 mg/g 85301-0203-15 Tucson 1.5 g FDA listed
Mineral Sunscreen tinted 80 mg/g; 38 mg/g 85302-0201-85 Face 85 g FDA listed
Matte Velvet Tint 80 mg/g; 38 mg/g 85334-0203-50 Brent 53 g FDA listed
Non Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85374-0202-50 BABYFACE 53 g FDA listed
Non Tinted Sunscreen 80 mg/g; 38 mg/g 85381-0202-50 VIDA 53 g FDA listed
AcneFix Non-Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85396-0202-50 ACNEFIX 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85414-0201-85 Hirschman, 85 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85442-0203-50 Saving 53 g FDA listed
Advanced Sun Protection 80 mg/g; 38 mg/g 85609-0203-50 HELLO 53 g FDA listed
Advanced Formula Tinted 80 mg/g; 38 mg/g 85883-0203-50 CR 53 g FDA listed
CoTZ Face Prime and Protect SPF 40 (Non-Tinted) 80 mg/g; 38 mg/g 58892-0348-45 Fallien 1 tube FDA listed
Tinted Mineral Sunscreen Spf 40 80 mg/g; 38 mg/g 85344-0203-50 DERMATOLOGY 53 g FDA listed
Non-Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85359-0202-50 R. 53 g FDA listed
Tinted Mineral Sun Protectant 80 mg/g; 38 mg/g 85459-0203-15 PANDA 1.5 g FDA listed
Tinted Physical Defense 80 mg/g; 38 mg/g 85499-0203-50 ATLANTA 53 g FDA listed
Silk Screen Tinted 80 mg/g; 38 mg/g 85644-0203-50 Skin 53 g FDA listed
Day Defense 80 mg/g; 38 mg/g 85695-0202-50 THE 53 g FDA listed
Non-Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85302-0202-50 Face 50 g FDA listed
Shaded 80 mg/g; 38 mg/g 85319-0201-85 Potency 85 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85329-0203-50 Lily 53 g FDA listed
Tinted Sunscreen 80 mg/g; 38 mg/g 85331-0203-15 Scottsdale 15 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85359-0203-50 R. 53 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85372-0203-50 Glow 53 g FDA listed
Prevention 80 mg/g; 38 mg/g 85463-0203-50 Noble 53 g FDA listed
ProtectME Tinted Mineral SPF 40 80 mg/g; 38 mg/g 85470-0203-50 PUREFECTION 53 g FDA listed
Mattifying Skin Primer 80 mg/g; 38 mg/g 85552-0202-50 SKIN 53 g FDA listed
Mattifying Mineral SPF40 Tinted 80 mg/g; 38 mg/g 85555-0203-50 ELIZA 53 g FDA listed
Mineral Sunscreen Non-Tinted 80 mg/g; 38 mg/g 85558-0202-50 LOTUS 53 g FDA listed
UV Shade tinted matte mineral SPF 40 80 mg/g; 38 mg/g 85632-0201-85 Joyce 85 g FDA listed
Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85696-0203-50 SCIENCE 53 g FDA listed
Tinted Sunscreen Face Primer 80 mg/g; 38 mg/g 85698-0203-50 LIV 53 g FDA listed
Sheer Tinted Sunscreen SPF40 80 mg/g; 38 mg/g 85706-0203-50 SIMPLICITY 53 g FDA listed
Daily Shade Matte Tinted 80 mg/g; 38 mg/g 85712-0203-50 BLISS 53 g FDA listed
Tinted Primer Mineral Sunscreen 80 mg/g; 38 mg/g 85715-0203-50 CECILIA 53 g FDA listed
UV Protection Veil Mineral Sunscreen, tinted 80 mg/g; 38 mg/g 85926-0203-15 ATHENA 15 g FDA listed
Emme Diane Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 81377-0203-50 Emme 53 g FDA listed
Clove Hill Tinted Mineral Sunscreen SPF 40 80 mg/g; 38 mg/g 82746-0203-50 Clove 53 g FDA listed
Non-Tinted Matte Mineral Sunscreen 80 mg/g; 38 mg/g 85330-0202-50 Skin 53 g FDA listed
Florida Babe Sport Tinted Mineral Sunscreen 80 mg/g; 38 mg/g 85337-0203-15 Tichy 1.5 g FDA listed
Mineral Sunscreen Dry Touch NT 80 mg/g; 38 mg/g 85431-0202-50 Cutis 53 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

🏛️
2021
On the market since
Apr 2021
📍
2026
Currently FDA-listed
5 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Titanium Dioxide, Zinc Oxide — the ingredient across all brands.

Top reported reactions

Exposure To Toxic Agent7
Product Contamination Chemical5
Acute Myeloid Leukaemia4
Malignant Melanoma4
Neoplasm Malignant4
Sunburn4
Application Site Rash3

Age at onset

Child1
Adolescent1
Adult7
Elderly2

Reporter sex

44 reports
Male · 24%
Female · 76%

Serious outcomes

Hospitalization7
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 11 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85591-0203-50 You're viewing this 53 g in 1 BOTTLE, PUMP (85591-203-50) 2021-04-16 Active

🧭 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 85591-203-50, 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: 85591-0203-50, written without dashes as 85591020350. 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 85591-0203-50, the first segment (85591) is the labeler code FDA assigned to JOSEPHINA RAMIREZ; the middle segment (0203) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (50) 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 JOSEPHINA RAMIREZ. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
JOSEPHINA RAMIREZ 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.
📄 FDA label 9 words

No readable label sections were found for this product.

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