HYVEE description, usages, side effects, indications, overdosage, supplying and lots more!

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HYVEE

HYVEE INC.
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

SODIUM FLUORIDE 0.05% (0.02% W/V FLUORIDE ION)

PURPOSE

ANTIGINGIVITIS/ANTIPLAQUE

USES

AIDS IN THE PREVENTION OF DENTAL CAVITIES.

WARNINGS

KEEP OUT OF REACH OF CHILDREN.

KEEP OUT OF REACH OF CHILDREN.

IF MORE THAN USED FOR RINSING IS ACCIDENTALLY SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

ADULTS AND CHILDREN 6 YEARS OF AGE AND OLDER: USE ONCE A DAY AFTER BRUSHING YOUR TEETH WITH TOOTHPASTE. VIGOROUSLY SWISH 10 ML OF RINSE BETWEEN YOUR TEETH FOR 1 MINUTE AND THEN SPIT OUT. DO NOT SWALLOW THE RINSE. DO NOT EAT OR DRINK FOR 30 MINUTES AFTER RINSING. SUPERVISE CHILDREN AS NECESSARY UNTIL CAPABLE OF USING WITHOUT SUPERVISION. CHILDREN UNDER 6 YEARS OF AGE: CONSULT A DENTIST OR DOCTOR.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE. COLD WEATHER MAY CLOUD THIS PRODUCT. ITS ANTISEPTIC PROPERTIES ARE NOT AFFECTED.

INACTIVE INGREDIENTS:

WATER, SORBITOL, PROPYLENE GLYCOL, SODIUM PHOSPHATE, POLYSORBATE 20, FLAVOR, POLOXAMER 407, SODIUM BENZOATE, POTASSIUM SORBATE, CALICUM DISODIUM EDTA, DISODIUM PHOSPHATE, SODIUM SACCHARIN, CETYLPYRIDINIUM CHLORIDE, MENTHOL, METHYL SALICYLATE, GREEN 3 (CI 42053), YELLOW 5 (CI 19140).

QUESTIONS OR COMMENTS?

1-800-289-8343

LABEL COPY

HYVEE

HYVEE

SODIUM FLUORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42507-554
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.5 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
propylene glycol
sodium phosphate
POLYSORBATE 20
POLOXAMER 407
SODIUM BENZOATE
POTASSIUM SORBATE
EDETATE CALCIUM DISODIUM ANHYDROUS
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
saccharin sodium
cetylpyridinium chloride
MENTHOL
methyl salicylate
FD&C GREEN NO. 3
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42507-554-16 474 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2013-09-12


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