Avant

Product NDC
53045-267
11-digit product format
530450267
Labeler code
53045
Product ID
53045-267_a3205319-0c52-4547-bc90-7d078f805894
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
LIQUID
Route
DENTAL
Labeler
Dharma Research, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-01-22
Substance
SODIUM FLUORIDE
Active strength
2 g/L
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Avant
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE2 g/L

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
251960Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
184bbe52-3909-45f6-b4d0-fe7849fabc1cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53045-267-64Avant1.9 L in 1 BOTTLE, PUMPLIQUID1.92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53045-267AVANT (SODIUM FLUORIDE) LIQUID [DHARMA RESEARCH, INC.]2Current NDC, Legacy NDC, 1 package rows20210126_184bbe52-3909-45f6-b4d0-fe7849fabc1c.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AvantSODIUM FLUORIDEDharma Research, Inc.184bbe52-3909-45f6-b4d0-fe7849fabc1c2021-01-25Warnings, Adverse reactionsExact identifier
ndc (product): 53045-267

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
251960sodium fluoride 2 % Oral RinsePSN184bbe52-3909-45f6-b4d0-fe7849fabc1c2
251960sodium fluoride 20 MG/ML MouthwashSCD184bbe52-3909-45f6-b4d0-fe7849fabc1c2
251960sodium fluoride 2 % Oral RinseSY184bbe52-3909-45f6-b4d0-fe7849fabc1c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53045-267-64530450267641.9 L in 1 BOTTLE, PUMP (53045-267-64) 1.9 l2021-01-220000-00-00NoNoCurrent