Medicine in DR Congo · official US FDA label
Coloprep (Lemon) 17.5g/3.13g/1.6g
Sulfate de sodium (sodium) · solution orale
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This is a US label.
The official US FDA label for sodium (published as SODIUM FLUORIDE), effective September 23, 2026, describes products sold in the United States. The medicine sold in DR Congo may differ in strength, form or approved uses: ask a pharmacist or a doctor.
Official US FDA label for sodium
Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. The full label on DailyMed.
Uses
Use Helps protect against cavities
Dosage
US dosage, for products sold in the United States. For a medicine bought in DR Congo, follow its box, its leaflet or your pharmacist.
Directions Adults & Children 6 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children 2 to 6 years: Use only a peasized amount and supervise child's brushing and rinsing (to minimize swallowing). Children under 2 years: Ask a dentist or physician.
Warnings and precautions
Warnings Keep out of the reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.
Where to find it in DR Congo
Not in stock in our pharmacies right now
Stock changes with every sale. Search by substance: a medicine with the same composition may be available.
Composition
| Substance | Strength | ATC code |
|---|---|---|
| Sulfate de sodium (sodium) | 17.5g/3.13g/1.6g | — |
Sources
- ●Labels: U.S. Food and Drug Administration, openFDA (public domain). Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. DailyMed.
- ●English names of substances: RxNorm, U.S. National Library of Medicine.
- ●Marketing authorizations: register of the ACOREP, DR Congo, version of February 4, 2026.
Public information, for reference only: it does not replace the advice of a pharmacist or a doctor. Vimpia writes nothing about how to use a medicine and translates nothing: the label is the US FDA's, unchanged; names, composition and authorizations come from the official sources above.