What is NDC 52000-108?

52000-108 is the product NDC for Advanced Whitening Anti Cavity Fluoride, Sodium monofluorophosphate .76 g/100g paste, listed with the FDA by Universal Distribution Center LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Advanced Whitening Anti Cavity Fluoride (Sodium Monofluorophosphate).

Universal Distribution Center LLC, NDC labeler code 52000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Advanced Whitening Anti Cavity Fluoride?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Advanced Whitening Anti Cavity Fluoride NDC 52000-108

NDC codes

FDA NDC Directory

Product NDC (as listed)52000-108Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52000-0108Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
52000-108-01	52000010801	181 g in 1 TUBE (52000-108-01)Marketed from May 18, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Advanced Whitening Anti Cavity Fluoride
Generic name (nonproprietary): sodium monofluorophosphate
Active ingredients: Sodium monofluorophosphate — .76 g/100g
Dosage form: Paste
Route: Dental
Labeler: Universal Distribution Center LLCNDC labeler code 52000
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 021
Marketing start: May 18, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 52000-108_ede5654c-864e-44c6-904b-ca2ac4532096SPL ID ede5654c-864e-44c6-904b-ca2ac4532096SPL set ID 8ea8a8d9-b7e4-468f-9a09-4ec634cbd80eRxCUI 545626UNII C810JCZ56Q

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N452000010801 followed by a unit qualifier and the quantity

Package 52000-0108-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 16, 2023.

Indications (excerpt from the label)

Uses builds increasing protection against painful sensitivity of teeth due to cold, heat, acids, sweets or contact. aids in the prevention of dental cavities.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 52000-108

What is NDC 52000-108?: 52000-108 is the product NDC for Advanced Whitening Anti Cavity Fluoride, Sodium monofluorophosphate .76 g/100g paste, listed with the FDA by Universal Distribution Center LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Advanced Whitening Anti Cavity Fluoride (Sodium Monofluorophosphate).
What is the active ingredient?: Sodium monofluorophosphate.
Who is the labeler?: Universal Distribution Center LLC, NDC labeler code 52000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Advanced Whitening Anti Cavity Fluoride?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 021

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 021
Product	Strength	Form · route	Labeler	Product NDC
3ECARE Dual FormulaWhiteningToothpastesodium fluoride	Sodium fluoride .155 g/100g	Paste, DentifriceDental	Hangzhou Namei Zhikang Technology Co., Ltd.	87514-003
Freshen Up twisted peppermintsodium fluoride	Sodium fluoride .24 g/100g	Gel, DentifriceDental	Dabur India Limited	87846-004
TheraBreath Anticavitysodium fluoride	Sodium fluoride .002 mg/10mL	RinseOral	Church & Dwight Co., Inc.	10237-265
PERIOE POP Complete Protection Prebiotic Mint Blastsodium fluoride	Sodium fluoride 1.4 mg/g	Paste, DentifriceDental	Tai Guk Pharm. Co., Ltd.	43136-603
Just For Kidsstannous fluoride	Stannous fluoride .969 mg/g	GelOral	Solventum US LLC	48878-4070
Brush Buddies Crayola Anticavity Fluoride Strawberrysodium fluoride	Sodium fluoride .05 g/100mL	LiquidOral	Kingkey MBC Life Technology Group Co.,Ltd	73928-038
Crest 3D White Advanced Luminous Mint Daily Whitening Upkeepsodium fluoride	Sodium fluoride 1.5 mg/g	Paste, DentifriceDental	The Procter & Gamble Manufacturing Company	84126-633
3ECARE Dual FormulaToothpastefor sensitiveteethpotassium nitrate sodium monofluorophosphate	Potassium nitrate 5 g/100g; Sodium monofluorophosphate 5 g/100g	Paste, DentifriceDental	Hangzhou Namei Zhikang Technology Co., Ltd.	87514-004
Freshen Up Vanilla Mintsodium fluoride	Sodium fluoride .24 g/100g	Gel, DentifriceDental	Dabur India Limited	87846-006
Alcohol-Free Anticavitysodium fluoride	Sodium fluoride .1 mg/mL	LiquidOral	Topco Associates LLC	36800-482
Anticavity Rinsesodium fluoride	Sodium fluoride .2 mg/mL	MouthwashOral	Meijer, Inc.	41250-004
Nature Mint Anticavitysodium monofluorophosphate	Sodium monofluorophosphate 7.6 mg/g	Paste, DentifriceDental	Bob Barker Company Inc.	53247-129
Brush Buddies Brbie Anticavity Fluoride Bubblegumsodium fluoride	Sodium fluoride .05 g/100mL	LiquidOral	Kingkey MBC Life Technology Group co., LTD.	73928-039
Anticavity Rinsesodium fluoride	Sodium fluoride .2 mg/mL	MouthwashOral	Retail Business Services, LLC	72476-204
Crest 3D White Advanced Charcoal with Stain-Blasting Foamsodium fluoride	Sodium fluoride 1.5 mg/g	Paste, DentifriceDental	The Procter & Gamble Manufacturing Company	84126-634
Freshen Upsodium fluoride	Sodium fluoride 24 mg/100g	Gel, DentifriceDental	DABUR INDIA LIMITED	87846-007
Colgate Total SF Clean Mintstannous fluoride	Stannous fluoride 1.1 mg/g	Paste, DentifriceDental	Colgate-Palmolive Company	35000-272
Anticavitysodium fluoride	Sodium fluoride .1 mg/mL	MouthwashOral	United Natural Foods, Inc. dba UNFI	41163-011
Anticavitysodium fluoride	Sodium fluoride .2 mg/mL	MouthwashOral	Walmart Inc.	49035-581
Maximum Securitysodium fluoride	Sodium fluoride 2.2 mg/g	Gel, DentifriceDental	Bob Barker Company Inc.	53247-130

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Advanced Whitening Anti Cavity Fluoride (Sodium monofluorophosphate) NDC 52000-108