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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 0.02% (0.01% W/V FLUORIDE ION)

PURPOSE

ANTIGINGIVITIS/ANTIPLAQUE

USES

TO HELP REDUCE AND PREVENT PLAQUE, GINGIVITIS.

WARNINGS

DO NOT USE IN CHILDREN UNDER 12 YEARS OF AGE.

KEEP OUT OF REACH OF CHILDREN.

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

DIRECTIONS

RINSE FULL STRENGTH FOR 30 SECONDS WITH 20 ML (2/3 FLUID OUNCE OR 4 TEASPOONFULS) MORNING AND NIGHT. DO NOT SWALLOW.

OTHER INFORMATION

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

INACTIVE INGREDIENTS:

WATER (AQUA), SORBITOL, ALCOHOL (21.6%), POLOXAMER 407, SODIUM LAURYL SULFATE, EUCALYPTOL, FLAVOR, METHYL SALICYLATE, THYMOL, PHOSPHORIC ACID, SUCRALOSE, MENTHOL, DISODIUM PHOSPHATE, RED 40 (CI 16035), BLUE 1 (ci 42090).

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:42507-552
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.2 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
ALCOHOL
POLOXAMER 407
SODIUM LAURYL SULFATE
EUCALYPTOL
methyl salicylate
THYMOL
phosphoric acid
Sucralose
MENTHOL
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
FD&C RED NO. 40
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42507-552-34 1000 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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