Drug labels

BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELON

SODIUM FLUORIDE · Kingkey MBC Life Technology Group co., LTD · ORAL

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
1b74ecc4-a1e6-348f-e063-6294a90a5894
ID
5dba5381-96a2-25e9-e063-6394a90a9dfd
Effective time
20261013
Version
3
SPL product data elements

BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELON SODIUM FLUORIDE SODIUM FLUORIDE FLUORIDE ION POLYOXYL 40 HYDROGENATED CASTOR OIL SUCRALOSE METHYL DIISOPROPYL PROPIONAMIDE POTASSIUM SORBATE GLYCERIN XYLITOL SACCHARIN SODIUM WATER CETYLPYRIDINIUM CHLORIDE FD&C YELLOW NO. 5 FD&C BLUE NO. 1 SORBITOL SODIUM BENZOATE CITRIC ACID MONOHYDRATE

Active ingredient
Active ingredient SODIUM FLUORIDE 0.02%
Purpose
Purpose (0.02% w/v fluoride ion)---------Anticavity
Indications and usage
Uses helps protect teeth against cavities
Keep out of reach of children

Warnings Keep out of reach of children under 6 years of age. If you accidentally swallow more than used for rinsing, seek professional help or contact a Poison Control Center immediately.

Dosage and administration

Directions Adults and children 6 years and older: Use daily after you brush your teeth with toothpaste. Rinse toothpaste from mouth prior to use. Shake well before each use. Twist and remove cap. Rinse or gargle for 30 seconds with 15 ml and spit out Do Not swallow the rinse. Do Not eat or drink for 30 minutes after rinsing. Supervise children as necessary. Children under 6 years of age, consult with a dentist or doctor.

Inactive ingredient

Inactive ingrdients WATER SORBITOL GLYCERIN XYLITOL POTASSIUM SORBATE SODIUM BENZOATE PEG-40 HYDROGENATED CASTOR OIL FLAVOR SODIUM SACCHARIN CETYLPYRIDINIUM CHLORIDE METHYL DIISOPROPYL PROPIONAMIDE SUCRALOSE CITRIC ACID FD&C Yellow No.5(CI 19140) FD&C Blue No.1(CI 42090)

Questions
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Package label principal display panel
label
Harmonized identifiers (openFDA)
Application number
M021
Brand name
BRUSH BUDDIES CRAYOLA ANTICAVITY FLUORIDE WATERMELON
Generic name
SODIUM FLUORIDE
Manufacturer name
Kingkey MBC Life Technology Group co., LTD
Product NDC
73928-041
Product type
HUMAN OTC DRUG
Route
ORAL
Substance name
SODIUM FLUORIDE
RxCUI
313029
SPL ID
5dba5381-96a2-25e9-e063-6394a90a9dfd
SPL set ID
1b74ecc4-a1e6-348f-e063-6294a90a5894
Package NDC
73928-041-01
Is original packager
true
Upc
0810147881208
UNII
8ZYQ1474W7
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.