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Natural Adult Fluoride Sodium monofluorophosphate .76 g/100g Paste, 1 tube — NDC 30142-0223-39 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Natural Adult Fluoride Sodium monofluorophosphate .76 g/100g Paste, 1 tube — NDC 30142-223-39 (Billing 30142-0223-39) · Product 30142-223

by Kroger · 1 TUBE in 1 CARTON (30142-223-39) / 155.9 g in 1 TUBE

NDC 30142-223-39 (billing 30142-0223-39) is a package of 1 tube of Natural Adult Fluoride Sodium monofluorophosphate .76 g/100g Paste from Kroger, marketed since Jun 2020 and currently FDA-listed. It is the main listing for product NDC 30142-223, its only package size.

NDC 30142-0223-39
🏷️ FDA NDC (as labeled) 30142-223-39 billing pads the product segment with a zero
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 30142-223-39
Product NDC 30142-223
11-digit billing NDC 30142022339
RxCUI 545626
UNII C810JCZ56Q
Application # M021
SPL Set ID a71c537e-39d9-1c3b-e053-2a95a90ac3ec
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-02
Route DENTAL
Dosage form PASTE
Substance SODIUM MONOFLUOROPHOSPHATE
Quick answers for NDC 30142-223-39
  • RxCUI (RxNorm): 545626
  • 11-digit billing NDC: 30142022339
Why two NDCs? The FDA registers this code as 30142-223-39 — 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 → 30142-0223-39. 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.

RxNorm drug class

This medicine belongs to the Caries prophylactic agents class.

Drug family (ATC) Caries prophylactic agents, Fluoride
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This is an over-the-counter toothpaste sold as a monograph drug product under FDA rules for its category. It contains sodium monofluorophosphate, a fluorine-based compound that is typically used in dental products to help strengthen tooth enamel and reduce the risk of cavities. The paste is applied topically to the teeth during brushing.

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.
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
30142-0223-39 30142-223-39 You're viewing this Main listing 1 TUBE in 1 CARTON (30142-223-39) / 155.9 g in 1 TUBE 2020-06-02 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
biotene 1.4 mg/g 00135-0577-01 Haleon 1 tube — — FDA listed —
Whitening .14 g/100g 11673-0385-09 Target 2 tubes — — FDA listed —
Kids Strawberry FTP .13 g/100g 11673-0441-01 Target 1 tube — — FDA listed —
Simple Truth Kids Flouride .76 g/100g 30142-0146-79 Kroger 119 g — — FDA listed —
Natural Adult Fluoride .76 g/100gthis 30142-0223-39 Kroger 1 tube — — FDA listed —
Colgate Revitalizing White 1 mg/g 35000-0017-46 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Cavity Protection Great Regular Flavor 1 mg/g 35000-0060-48 Colgate-Palmolive 1 tube — — FDA listed —
Hello Whipped Peppermint Stick Flavor 1.1 mg/g 35000-0512-10 Colgate-Palmolive 1 tube — — FDA listed —
Hello Whipped Mellow Mint Dream Flavor 1.1 mg/g 35000-0513-10 Colgate-Palmolive 1 tube — — FDA listed —
Hello Activated Charcoal 1.1 mg/g 35000-0678-10 Colgate-Palmolive 1 tube — — Discontinued —
Hello Naturally Whitening 1.1 mg/g 35000-0682-10 COLGATE 1 tube — — FDA listed —
Colgate Optic White Pro Series Stain Prevention 1.1 mg/g 35000-0747-16 Colgate-Palmolive 1 tube — — Discontinued —
Colgate Optic White Stain Prevention 1 mg/g 35000-0893-43 Colgate-Palmolive 1 tube — — Discontinued —
COLGATE Great Regular Flavor 1 mg/g 35000-0913-01 Colgate-Palmolive 1 tube — — FDA listed —
ULTRA BRITE Baking Soda and Peroxide Whitening Cool Mint 1 mg/g 35000-0916-60 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Sparkling White Mint Zing 1 mg/g 35000-0919-46 Colgate-Palmolive 1 tube — — Discontinued —
COLGATE Baking Soda and Peroxide Whitening Brisk Mint 1 mg/g 35000-0959-46 Colgate-Palmolive 1 tube — — Discontinued —
Colgate Optic White Platinum Stain-Less 1 mg/g 35000-0973-32 Colgate-Palmolive 1 tube — — Discontinued —
Colgate Essentials 1 mg/g 35000-0974-46 Colgate-Palmolive 1 tube — — Discontinued —
Colgate Optic White Advanced Icy Fresh 1 mg/g 35000-0977-32 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Optic White Advanced Sparkling White 1 mg/g 35000-0978-14 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Optic White Renewal High Impact White 1 mg/g 35000-0982-15 Colgate-Palmolive 1 tube — — Discontinued —
MediChoice Fluoride 7.6 mg/g 39892-0602-01 O&M 17 g — — FDA listed —
Natures Promise Childrens Fluoride Strawberry .13 g/100g 41520-0724-29 Foodhold 119 g — — FDA listed —
Charm Tex FLUORIDE .1 g/100g 42086-0051-01 Jiangsu 720 tubes — — FDA listed —
United Dental Kit 42509-0134-01 Wessco 1 kit — — FDA listed —
Colgate Anticavity 7.6 mg/g 42555-0060-45 Colgate-Palmolive 10 g — — FDA listed —
365 Everyday Value Cavity Fighting and Whitening .13 g/100g 42681-5002-09 Whole 1 tube — — Discontinued —
365 Everyday Value Kids Flouride .13 g/100g 42681-5276-09 Whole 119 g — — FDA listed —
Tom Whole Care Peppermint fights cavities whitening fresh breath helps fight tartar 1.4 mg/g 51009-0202-04 Tom's 1 tube — — FDA listed —
Toms Whole Care Spearmint fights cavities whitening fresh breath helps fight tartar 1.4 mg/g 51009-0203-04 Tom's 1 tube — — FDA listed —
Toms Wicked Fresh Cool Peppermint fresh breath / cavity protection 1.4 mg/g 51009-0205-47 Tom's 1 tube — — Discontinued —
Toms Wicked Fresh Spearmint Ice fresh breath / cavity protection 1.4 mg/g 51009-0206-47 Tom's 1 tube — — Discontinued —
Toms Whole Care Cinnamon Clove FIGHTS CAVITIES WHITENING FRESH BREATH HELPS FIGHT TARTAR 1.4 mg/g 51009-0219-04 Tom's 1 tube — — FDA listed —
Toms Kids Watermelon Wiggle 1 mg/g 51009-0854-42 Tom's 119 g — — Discontinued —
Toms Of Maine Whole Care Spearmint 1 mg/g 51009-0857-69 Tom's 1 tube — — FDA listed —
Toms Of Maine Whole Care Spearmint 1 mg/g 51009-0858-69 Tom's 1 tube — — FDA listed —
Toms Of Maine Wicked Fresh Cool Peppermint 1 mg/g 51009-0859-07 Tom's 1 tube — — FDA listed —
Toms Of Maine Wicked Fresh Spearmint Ice 1 mg/g 51009-0860-07 Tom's 1 tube — — FDA listed —
Toms Of Maine Whole Care Wintermint 1 mg/g 51009-0902-40 Tom's 1 tube — — FDA listed —
Toms Of Maine Kids Silly Strawberry 1 mg/g 51009-0910-10 Tom's 1 tube — — Discontinued —
Toms Of Maine Kids Outrageous Orange Mango 1 mg/g 51009-0911-51 Tom's 144 g — — FDA listed —
Toms Of Maine Wicked Cool Mild Mint 1 mg/g 51009-0912-51 Tom's 144 g — — FDA listed —
Freshmint Anticavity Fluoride 7.6 mg/g 51824-0067-01 New 17 g — — FDA listed —
Anti Cavity Fluoride .76 g/100g 52000-0107-01 Universal 181 g — — FDA listed —
Advanced Whitening Anti Cavity Fluoride .76 g/100g 52000-0108-01 Universal 181 g — — FDA listed —
Universal Anti-Cavity Fluoride .76 g/100g 52000-0111-01 Universal 181 g — — FDA listed —
Universal Advanced Whitening Anti-Cavity Fluoride .76 g/100g 52000-0112-01 Universal 181 g — — FDA listed —
Medpride 7.6 mg/g 52410-9005-03 Shield 42.5 g — — FDA listed —
PERIOSCIENCES HYDRATING AO Pro 1.3 mg/mL 53238-0003-90 PERIOSCIENCES 1 tube — — FDA listed —
Nature Mint Anticavity 7.6 mg/g 53247-0129-01 Bob 7.94 g — — FDA listed —
Nature Mint Anticavity 7.6 mg/g 53247-0144-01 Bob 7.94 g — — Discontinued —
SparkleFresh Flouride Toothpaste 1 mg/g 53329-0083-21 Medline 42.5 g — — FDA listed —
Rexall Travel Toothbrush and Tooth-paste 55910-0087-01 Old 1 kit — — FDA listed —
Colgate Anticavity Kit 7.6 mg/g 56153-0001-05 Ming 1 tube — — FDA listed —
Colgate Anticavity Kit 7.6 mg/g 56153-0002-05 Ming 1 tube — — FDA listed —
First Class Kit 7.6 mg/g 58701-0001-10 American 1 tube — — FDA listed —
Business Class Kit 7.6 mg/g 58701-0002-10 American 1 tube — — FDA listed —
United Airlines Business Class Kit 7.6 mg/g 58733-0001-10 United 1 tube — — FDA listed —
smart way MINT cavity protection .13 g/100g 59450-0010-01 The 1 tube — — FDA listed —
AP-24 Whitening 7.6 mg/g 62839-1155-01 NSE 110 g — — FDA listed —
COLGATE Great Regular Flavor 1 mg/g 65954-0060-01 Mission 1 tube — — FDA listed —
Colgate ULTRA BRITE Baking Soda and Peroxide Whitening 1.1 mg/g 65954-0063-60 Mission 1 tube — — FDA listed —
Colgate Sparkling White Mint Zing 1 mg/g 65954-0068-48 Mission 1 tube — — FDA listed —
COLGATE Baking Soda and Peroxide Whitening Brisk Mint 1 mg/g 65954-0765-48 Mission 1 tube — — FDA listed —
Colgate Baking Soda and Peroxide Whitening Oxygen Bubbles Frosty Mint 1 mg/g 65954-0768-35 Mission 3 tubes — — FDA listed —
Colgate Optic White Platinum Stain-Less 1 mg/g 65954-0785-32 Mission 1 tube — — FDA listed —
Colgate Essentials 1 mg/g 65954-0786-46 Mission 1 tube — — FDA listed —
Colgate Great Regular Flavor 1 mg/g 67751-0118-01 Navajo 1 tube — — FDA listed —
Morning Fresh 76 mg/g 67777-0175-11 Dynarex 1 tube — — FDA listed —
Sodium Monofluorophosphate 760 mg/g 67777-0181-02 Dynarex 144 tubes — — FDA listed —
Morning Fresh Mint Toothpaste, with Fluoride 1.3 mg/mL 67777-0190-03 Dynarex 144 tubes — — FDA listed —
Fluoride .76 g/g 68599-9571-01 McKesson 1 g — — FDA listed —
Murchison Hume Dental Kit 69491-0034-01 Buzz 1 kit — — FDA listed —
Ipana Wintergreen Fluoride .1 g/100g 69510-0010-19 Maxill 1 tube — — FDA listed —
Ipana Bucky Beaver Bubble Gum Childrens Fluoride .1 g/100g 69510-0020-19 Maxill 1 tube — — FDA listed —
Listerine Essential Care 1.3 mg/g 69968-0701-04 Kenvue 1 tube — — FDA listed —
Brush Buddies Value 2 pack Whitening .76 g/100g 70108-0030-01 Ashtel 2 tubes — — FDA listed —
Brush Buddies 2 VALUE PACK CAVITY PROTECTION ANTI-CAVITY FLUORIDE .15 g/100g 70108-0185-01 Ashtel 2 tubes — — FDA listed —
Charm Tex FLUORIDE .1 g/100g 71035-0001-01 Yangzhou 720 tubes — — FDA listed —
dentalux ANTI-CAVITY FLUORIDE .13 g/100g 71141-0186-10 Lidl 1 tube — — FDA listed —
Orazen .1 g/100g 71927-0102-01 Orazen 1 tube — — FDA listed —
Colgate 5g Toothbrush Kit 72845-0000-00 Wuhan 1 kit — — FDA listed —
Colgate Anticavity 73234-0040-00 MING 1 kit — — FDA listed —
Cloveden Tooth .76 g/100g 73242-1112-02 DONG 1 tube — — FDA listed —
White Glo Micellar 73656-0003-00 WHITE 1 kit — — FDA listed —
White Glo Bio-Enzyme 73656-0005-00 WHITE 1 kit — — FDA listed —
White Glo Professional Choice 73656-0007-00 WHITE 1 kit — — FDA listed —
White Glo Charcoal 73656-0009-00 WHITE 1 kit — — FDA listed —
White Glo Maximum White Charcoal 73656-0013-00 WHITE 1 kit — — FDA listed —
White Glo Instant White 73656-0015-00 WHITE 1 kit — — FDA listed —
White Glo Mouthwash Protection 73656-0017-00 WHITE 1 kit — — FDA listed —
White Glo Activated Charcoal Twin Pack 73656-0020-00 WHITE 1 kit — — FDA listed —
White Glo Professional Choice Twin Pack 73656-0024-00 WHITE 1 kit — — FDA listed —
White Glo Advantage Anticavity Fluoride Purple 7.6 mg/g 73656-0026-00 WHITE 1 tube — — FDA listed —
White Glo Advantage Anticavity Professional Whitening 7.6 mg/g 73656-0027-00 WHITE 1 tube — — FDA listed —
White Glo Instant White Blue Foam Optical Enhancers Fluoride Anticavity Value 2 pack and Toothbrush 73656-0028-00 WHITE 1 kit — — FDA listed —
White Glo Coffee and Tea Stain Remover Fluoride Anticavity 73656-0030-00 WHITE 1 kit — — FDA listed —
Optimax Anticavity Fluoride Watermelon 7.6 mg/g 73656-0032-00 WHITE 1 tube — — FDA listed —
Optimax Anticavity Fluoride Cotton Candy 7.6 mg/g 73656-0033-00 WHITE 1 tube — — FDA listed —
Optimax Purple Anticavity Fluoride 73656-0034-00 WHITE 1 kit — — FDA listed —
Optimax Professional Whitening Anticavity Fluoride 73656-0036-00 WHITE 1 kit — — FDA listed —
Optimax Professional Whitening Anticavity Fluoride 73656-0038-00 WHITE 1 kit — — FDA listed —
Optimax Purple Anticavity Fluoride 73656-0039-00 WHITE 1 kit — — FDA listed —
White Glo Charcoal Baking Soda Maximum White Fluoride Anticavity 73656-0041-00 White 1 kit — — FDA listed —
White Glo Coffee and Tea Stain Remover Fluoride Anticavity 73656-0042-00 White 1 kit — — FDA listed —
White Glo Professional Choice Fluoride Anticavity 7.6 mg/g 73656-0043-00 White 2 tubes — — FDA listed —
White Glo Mouthwash Protect Fluoride Anticavity 73656-0044-00 White 1 kit — — FDA listed —
White Glo Extreme White Whitening 7.6 mg/g 73656-0046-00 White 2 tubes — — FDA listed —
White Glo Purple Color Corrector Fluoride Anticavity 7.6 mg/g 73656-0047-00 White 2 tubes — — FDA listed —
Optimax Anticavity Fluoride Bubblegum 7.6 mg/g 73656-0048-00 White 1 tube — — FDA listed —
Optimax Anticavity Fluoride Raspberry 7.6 mg/g 73656-0049-00 White 1 tube — — FDA listed —
Freshen Up .76 g/100g 77782-0005-20 MKJ 2 bottles — — FDA listed —
Colgate Anticavity 79940-0010-00 FORMIA 1 kit — — FDA listed —
Colgate Anticavity 79940-0012-00 FORMIA 1 kit — — FDA listed —
Colgate Anticavity 79940-0013-00 FORMIA 1 kit — — FDA listed —
Coffe Tea Stain Remover Tooth .76 g/100g 82168-0001-01 Guangzhou 150 g — — FDA listed —
Instant Whitening .76 g/100g 82168-0002-01 Guangzhou 150 g — — FDA listed —
Professional Choice .76 g/100g 82168-0003-01 Guangzhou 150 g — — FDA listed —
Professional whitening tooth .76 g/100g 82168-0004-01 Guangzhou 100 g — — FDA listed —
purple tooth .76 g/100g 82168-0005-01 Guangzhou 100 g — — FDA listed —
Zohar Fluoride Anti Cavity Coolmint Flavour 7.6 mg/g 84045-0004-00 ZOHAR 1 tube — — Discontinued —
Zohar Fluoride Anti-Cavity Regular Mint Flavour 7.6 mg/g 84045-0005-00 ZOHAR 1 tube — — Discontinued —
Zohar Fluoride Anti Cavity Fresh Mint Flavor 7.6 mg/g 84045-0006-00 ZOHAR 1 tube — — Discontinued —
DeCure 7.6 mg/g 84132-0100-10 Scope 10 g — — FDA listed —
Carekon Anti-Cavity Fluoride .76 g/100g 84345-0086-01 Hunan 1 tube — — FDA listed —
Nature Mint Anti cavity Fluoride .1 g/100g 85891-0009-01 SPARROW 720 tubes — — Discontinued —
Fluoride Anticavity,Toothpaste .76 g 87576-0332-02 Shulisa 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.

Availability & generic status

🏛️
2020
On the market since
Jun 2020
📍
2026
Currently FDA-listed
6 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.

What it looks like

Color white
FlavorMint
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 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 H0G9379FGK
    Calcium carbonate is a white mineral powder used as a filler and buffering agent in medicines. It helps give tablets their bulk and size while neutralizing stomach acid in some formulations.
  • UNII 5C69YCD2YJ
    Carrageenan is a natural thickener and stabilizer extracted from red seaweed. It's used in medicines to create gel-like textures, improve consistency, and help keep ingredients from separating 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 Y6O7T4G8P9
    Hydrated silica is a fine powder form of silicon dioxide with absorbed water. It works as an anti-caking agent and absorbent in medicines, helping powders stay free-flowing and preventing clumping.
  • UNII 8MDF5V39QO
    A white powder form of baking soda that acts as a buffer and pH regulator in medicines. It helps maintain the right acid-base balance and may aid tablet disintegration.
  • UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • 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.
  • UNII VCQ006KQ1E
    Xylitol is a naturally occurring sugar alcohol derived from plants. It's used in medicines as a sweetener, bulking agent, and to improve taste, especially in liquid formulations and chewable tablets.
  • UNII K72I3DEX9B
    Zinc citrate is a zinc salt combined with citric acid. It's used in medicines as a source of zinc and sometimes as a buffer to help maintain the product's pH balance.

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

The official label also statesglycerin, water, calcium carbonate, hydrated silica, xylitol, sodium bicarbonate, carrageenan, sodium lauroyl sarcosinate, flavor, zinc citrate, benzyl alcohol

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

LabelerKroger
FDA applicationM021 (OTC MONOGRAPH DRUG)
Labeler code30142
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio39 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.

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 8 words ▾

Uses aids in the prevention of dental cavities

⏱️ Dosage and Administration 71 words ▾

Directions adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least twice per day, or as directed by a dentist or doctor. * instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing) * supervise children as necessary until capable of using without supervision * children under 2 years of age: Consult a dentist or doctor.

⚠️ Warnings 32 words ▾

Keep out of reach of children under 6 years of age. If more than is swallowed for brushing si accidentally swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 14 words ▾

Active ingredient Purpose Sodium monofluorophosphate 0/76% (0.13% w/v fluoride ion) . . . Anticavity

🧪 Inactive Ingredients 18 words ▾

glycerin, water, calcium carbonate, hydrated silica, xylitol, sodium bicarbonate, carrageenan, sodium lauroyl sarcosinate, flavor, zinc citrate, benzyl alcohol

🎯 Purpose 8 words ▾

Uses aids in the prevention of dental cavities

📄 Keep Out of Reach of Children 32 words ▾

Keep out of reach of children under 6 years of age. If more than is swallowed for brushing si accidentally swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

Carton Artwork

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

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 Natural Adult Fluoride (this brand).

Top reported reactions

Pelvic Fracture2
Abdominal Discomfort1
Abdominal Pain Upper1
Bone Metabolism Disorder1
Burning Sensation1
Cardiac Disorder1
Chest Pain1

Age at onset

Adult1

Reporter sex

8 reports
Male · 75%
Female · 25%

Serious outcomes

Hospitalization3
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2025 2026 1 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.

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 30142-223-39, 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: 30142-0223-39, written without dashes as 30142022339. 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 30142-0223-39, the first segment (30142) is the labeler code FDA assigned to Kroger; the middle segment (0223) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (39) 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 Kroger. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kroger 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.
← 30142-0221-24 · THE 30142-0232-15 · KROGER →
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.