PERIOE KAKAO KIDS Strawberry Sodium Fluoride 1.3 mg/g Paste, Dentifrice — NDC 53208-461-60 (Billing 53208-0461-60)
This is a package of PERIOE KAKAO KIDS Strawberry Sodium Fluoride 1.3 mg/g Paste, Dentifrice from LG HOUSEHOLD & HEALTH CARE LTD., marketed since Nov 2025 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 53208-461-60 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 53208 labeler · 461 product · 60 package
- Package marketed since
- Nov 30, 2025
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 5320846160 0
- 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 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Caries prophylactic agents class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
This is a strawberry-flavored toothpaste for children that contains sodium fluoride as its active ingredient. Sodium fluoride is commonly used in dental products to help strengthen tooth enamel and reduce the formation of cavities. The paste is applied directly to the teeth during brushing. This product is marketed as an over-the-counter drug under the FDA's monograph rules for oral care products.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 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 3, 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 |
|---|---|---|---|---|
| 53208-0461-60 You're viewing this Main listing | 1 BOTTLE, PUMP in 1 CARTON / 160 g in 1 BOTTLE, PUMP | 2025-11-30 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 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 1, 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 9E8X80D2L0
A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
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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.
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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 91D9GV0Z28
A mineral salt made from calcium and phosphate. It acts as a filler to add bulk to the tablet or capsule, and helps bind ingredients together so the medicine holds its shape.
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UNII 25X51I8RD4
Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
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UNII TUF2IVW3M2
Poloxamer 407 is a synthetic polymer made from ethylene oxide and propylene oxide. In medicines, it acts as a thickener, emulsifier, and solubilizer to help mix ingredients and create the right texture.
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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 285CYO341L
Sodium polyacrylate is a synthetic polymer that absorbs and holds water. In medicines, it acts as a disintegrant, helping tablets break apart quickly in the stomach, and as a binder, holding tablet ingredients together.
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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 06XEA2VD56
Sorbitan oleate is an emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in the medicine.
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UNII 96K6UQ3ZD4
Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
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UNII O352864B8Z
A sodium salt compound used in medicines as a buffering agent to maintain pH stability and as a chelating agent to prevent unwanted chemical reactions during storage and mixing.
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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.
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UNII TTV12P4NEE
Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.
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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.
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UNII H92E6QA4FV
Zinc stearate is a fine white powder made from zinc and stearic acid. It works as a lubricant and glidant to help the tablet or capsule move smoothly through manufacturing equipment and prevents sticking.
17 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 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 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 LG HOUSEHOLD & HEALTH CARE LTD. labeler code 53208
- DOMINAS DARK SPOT TINTED SUNSCREEN Octisalate, Octocrylene, Titanium Dioxide, Zinc Oxide 2.5 g/100g; 1.53 g/100g; 4 g/100g; 8.73 g/100g Cream NDC 53208-302-02
- GANGNAM Glow Day Shield Perfect Sunscreen SPF 50 Octisalate, Octocrylene, Titanium Dioxide, Zinc Oxide 4 g/50mL; 8.73 g/50mL; 2.5 g/50mL; 1.53 g/50mL Cream NDC 53208-401-50
- Gangnam Glow Sunscreen 50 Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene 90 mg/mL; 45 mg/mL; 27 mg/mL; 70 mg/mL; 90 mg/mL Cream NDC 53208-411-50
- AVON BEYOND GLOW SUN MILK Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene 90 mg/mL; 45 mg/mL; 27 mg/mL; 70 mg/mL; 90 mg/mL Cream NDC 53208-421-52
- AVON BEYOND GLOW SUN MOISTURIZER Avobenzone, Homosalate, Octisalate, Octocrylene 27 mg/mL; 45 mg/mL; 90 mg/mL; 90 mg/mL Cream NDC 53208-422-50
- Sum 37 Micro Active Daily Moisture Sunscreen Avobenzone, Homosalate, Octisalate, Octocrylene 45 mg/mL; 90 mg/mL; 27 mg/mL; 90 mg/mL Cream NDC 53208-440-02
- EUTHYMOL Extraordinary Pink Whitening Sodium Fluoride 1.6 mg/g Paste, Dentifrice NDC 53208-561-06
- EUTHYMOL Extraordinary Pink Whitening Sodium Fluoride 1.6 mg/g Paste, Dentifrice NDC 53208-562-20
- Euthymol Whitening Purple Corrector Sodium Fluoride 1.5 mg/g Paste, Dentifrice NDC 53208-563-20
- Euthymol Whitening Sodium Fluoride 1.5 mg/g Paste, Dentifrice NDC 53208-566-45
- EUTHYMOL WHITENING SET Sodium Fluoride Kit NDC 53208-568-00
- EUTHYMOL WHITENING TRAVEL Sodium Fluoride Kit NDC 53208-569-00
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Use helps protect against cavities
⏱️ Dosage and Administration ▾
Directions Do not swallow. If you accidentally swallow more than used for brushing, seek professional assistance or contact a poison control center right away. If an allergic reaction develops, discontinue use immediately.
⚠️ Warnings ▾
Keep out of reach of children Keep out of reach of children under 6 years of age. Directions Do not swallow. If you accidentally swallow more than used for brushing, seek professional assistance or contact a poison control center right away. If an allergic reaction develops, discontinue use immediately.
🧪 Active Ingredient ▾
Active Ingredients Sodium Fluoride 0.243% (0.13% w/v fluoride ion)
🧪 Inactive Ingredients ▾
Inactive ingredients GLYCERIN, WATER, HYDRATED SILICA, SODIUM LAURYL SULFATE, FLAVOR, XANTHAN GUM, TETRASODIUM PYROPHOSPHATE, POLOXAMER 407, SODIUM POLYACRYLATE, ZINC STEARATE, SODIUM SACCHARIN, SORBITAN OLEATE, TITANIUM DIOXIDE, SUCRALOSE, HYDROXYAPATITE, NIACINAMIDE, TOCOPHERYL ACETATE, XYLITOL
🎯 Purpose ▾
Purpose Anticavity toothpaste
📄 Keep Out of Reach of Children ▾
Keep out of reach of children Keep out of reach of children under 6 years of age.
📄 Questions or Comments ▾
Questions? 1-866-993-4709
📖 Instructions for Use ▾
Directions adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directly 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 years: ask a dentist.
📄 Package Label / Principal Display Panel ▾
Bottle Carton
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 | — Not published for this NDC No photo available yet for this listing. |
| 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. |