ATOMY PROPOLIS TOOTHPAS TE 50G- sodium monofluorophosphate, sodium fluoride paste, dentifrice

Country: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Virkt innihaldsefni:

SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O), SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)

Fáanlegur frá:

ATOMY CO., LTD.

Stjórnsýsluleið:

ORAL

Gerð lyfseðils:

OTC DRUG

Ábendingar:

Purpose: Anticaries Uses: Aids in the prevention of dental cavities.

Leyfisstaða:

OTC monograph final

Vara einkenni

ATOMY PROPOLIS TOOTHPAS TE 50G- SODIUM MONOFLUOROPHOSPHATE, SODIUM
FLUORIDE PASTE, DENTIFRICE
ATOMY CO., LTD.
----------
Active Ingredient: Sodium Monofluorophosphate 0.16%, Sodium Fluoride
0.10%
Inactive Ingredients: SORBITOL, HYDRATED SILICA, WATER, SILICA, SODIUM
LAURYL
SULFATE, TETRASODIUM PYROPHOSPHATE, PEG-32, CELLULOSE GUM, CITRUS
FLAVOR, CITRUS AURANTIUM DULCIS(ORANGE) PEEL OIL, MINT FLAVOR, SODIUM
SACCHARIN, XYLITOL, CAMELLIA SINENSIS EXTRACT, MENTHOL, PROPOLIS
EXTRACT
Purpose: Anticaries
Warnings:
Ask a doctor before use if you have:
Bleeding or redness lasting more than 2 weeks.
Pain, swelling, pus, loose teeth, or more spacing between teeth.
These may be signs of periodontitis, a serious form of gum disease.
Keep out of 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 right away.
Directions:
1) Adults and children 2 years of age and older: Brush teeth throughly
preferably after
each meal or at least twice a day or as directed by a dentist or
doctor. 2) Children under
6 years: To minimize swallowing, use a pea-sized amount and supervise
brushing until
good habits are established. 3) Children under 2 years: Consult a
dentist or doctor.
Uses:
Aids in the prevention of dental cavities.
Questions?
1-253-946-2344
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ATOMY PROPOLIS TOOTHPAS TE 50G
sodium monofluorophosphate, sodium fluoride paste, dentifrice
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:52257-1380
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION -
UNII:Q80VPU408O)
FLUORIDE ION
0.08 g
in 50 g
0.05 g
ATOMY CO., LTD.
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)
FLUORIDE ION
0.05 g
in 50 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (U