Crest Cavity Protection Regular Sodium Fluoride 1.5 mg/g Paste, Dentifrice — NDC 67751-124-01 (Billing 67751-0124-01)
This is a package of Crest Cavity Protection Regular Sodium Fluoride 1.5 mg/g Paste, Dentifrice from Navajo Manufacturing Company Inc., marketed since Aug 1984 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.
NDC database record
One package, one record: these facts belong to NDC 67751-124-01 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 67751 labeler · 124 product · 01 package
- Package marketed since
- Nov 26, 1999
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 6775112401 1
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 891775
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
RxNorm drug class
This medicine belongs to the Caries prophylactic agents class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 8, 2026
Clinical
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Read the full MedlinePlus article ↗This is an over-the-counter toothpaste containing sodium fluoride, an ingredient typically used in dental products to help protect teeth from decay. Fluoride functions as a topical agent that strengthens tooth enamel and is commonly found in toothpastes marketed for cavity prevention. The product is applied by brushing onto the teeth and is regulated under the FDA's over-the-counter monograph rules for anticavity dentifrice products.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per g | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 9, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 67751-0124-01 You're viewing this Main listing | 1 TUBE in 1 BLISTER PACK / 24 g in 1 TUBE | 1999-11-26 | — | Active |
| 67751-0124-02 67751-124-02 | 1 TUBE in 1 BLISTER PACK / 24 g in 1 TUBE | 1999-11-26 | — | Active |
Pack size FAQ
What quantity is in this package?
What NDC number is used to bill for this package of Crest Cavity Protection Regular Sodium Fluoride 1.5 mg/g Paste, Dentifrice?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
What it looks like
Where does this data come from?
- FDA label on DailyMed · label index refreshed Oct 8, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
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UNII K679OBS311
Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
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UNII 0A5MM307FC
A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
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UNII H3R47K3TBD
FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
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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.
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UNII SB8ZUX40TY
Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
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UNII 368GB5141J
A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
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UNII SE337SVY37
A mineral salt used as a buffer to help maintain the medicine's pH level and prevent breakdown of active ingredients. It also acts as a thickening agent in liquid formulations.
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UNII SX01TZO3QZ
A mineral salt made from sodium and phosphate. It acts as a buffer to maintain the medicine's pH level and can help bind ingredients together in solid dosage forms.
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UNII 506T60A25R
Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
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UNII 15FIX9V2JP
Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
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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.
11 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Navajo Manufacturing Company Inc. labeler code 67751
- Caseys Antimicrobial Hand Sanitizer ETHYL ALCOHOL 70 mL/100mL Gel NDC 67751-071-01
- Handy Solutions Hand Sanitizer ALCOHOL 70 mL/100mL Liquid NDC 67751-086-01
- Handy Solutions Crest Complete MULTI-BENEFIT WHITENING plus Scope SODIUM FLUORIDE 1.5 mg/g Paste, Dentifrice NDC 67751-095-01
- Colgate Great Regular Flavor SODIUM MONOFLUOROPHOSPHATE 1 mg/g Paste, Dentifrice NDC 67751-118-01
- Excedrin Extra Strength Pain Reliever Acetaminophen, Aspirin (NSAID), and Caffeine 250 mg; 250 mg; 65 mg Tablet, Film Coated NDC 67751-119-01
- Motrin IB IBUPROFEN 200 mg Tablet, Film Coated NDC 67751-120-01
- Flanax Pain Reliever/Fever Reducer Naproxen Sodium 220 mg Tablet NDC 67751-125-01
- Bayer Genuine Aspirin 325 mg Tablet NDC 67751-129-01
- Refresh Tears Lubricant CARBOXYMETHYLCELLULOSE SODIUM 5 mg/mL Solution/ Drops NDC 67751-130-01
- HANDY SOLUTIONS DOVE COOL ESSENTIAL CUCUMBER AND GREEN TEA SCENT ANTI-PERSPIRANT Aluminum Zirconium Tetrachlorohydrex GLY 14.8 g/100g Stick NDC 67751-134-01
- Aleve naproxen sodium 220 mg Tablet NDC 67751-144-01
- Midol ACETAMINOPHEN, CAFFEINE, and PYRILAMINE MALEATE 500 mg; 60 mg; 15 mg Tablet NDC 67751-145-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Use helps protect teeth and roots against cavities
⏱️ Dosage and Administration ▾
Directions adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist do not swallow to minimize swallowing use a pea-sized amount in children under 6 supervise children's brushing until good habits are established children under 2 yrs.: ask a dentist
⚠️ Warnings ▾
Warnings Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Sodium fluoride 0.243% (0.15% w/v fluoride ion)
🧪 Inactive Ingredients ▾
Inactive ingredients sorbitol, water, hydrated silica, sodium lauryl sulfate, trisodium phosphate, flavor, cellulose gum, sodium phosphate, carbomer, sodium saccharin, titanium dioxide, blue 1
🎯 Purpose ▾
Purpose Anticavity toothpaste
📄 Keep Out of Reach of Children ▾
Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions? 1-800-492-7378
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL 29985 V5 27066 V7
Reported adverse events (FAERS)
Top reported reactions
Age at onset
Reporter sex
Serious outcomes
Where does this data come from?
About this NDC listing & data coverage
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. |