ACT Total Care Sensitive Anticavity Tropical Mouth description, usages, side effects, indications, overdosage, supplying and lots more!

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ACT Total Care Sensitive Anticavity Tropical Mouth

Chattem, Inc.

ACT Total Care Sensitive Anticavity Mouth Rinse Tropical




FULL PRESCRIBING INFORMATION

Drug Facts

Sodium fluoride 0.02% (0.009% w/v fluoride ion)

Anticavity

  • aids in the prevention of dental cavities

If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

adults and children 6 years of age and older:

  • use twice a day after brushing your teeth with a toothpaste
  • remove cap
  • pour 10 milliliters (10 mL mark on inside of cap); do not fill above 10 mL mark
  • vigorously swish 10 milliliters 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
  • instruct children under 12 years of age in good rinsing habits (to minimize swallowing)
  • supervise children as necessary until capable of using without supervision

children under 6 years of age: consult a dentist or doctor

if safety seal is broken or missing

water, glycerin, sorbitol, xylitol, poloxamer 407, betaine, propylene glycol, bisabolol, carnosine, zingiber officinale (ginger) root extract, angelica polymorpha sinensis root extract, lonicera japonica (honeysuckle) flower extract, pueraria lobata root extract, PEG-14M, PEG-160M, flavors, sodium benzoate, potassium sorbate, sodium phosphate, disodium phosphate, polysorbate 20, lactic acid, calcium disodium EDTA, cetylpyridinium chloride, red 40, yellow 10 (283-181)

Learn more at www.ACTFLUORIDE.com

#1 DENTIST RECOMMENDED
FLUORIDE BRAND
ACT® 
TOTAL CARE
ANTICAVITY FLUORIDE MOUTHWASH
Sensitive FORMULA
alcohol free
Tropical
Sodium Fluoride 0.02%
18 fl oz (532 mL)

ACT Total Care Sensitive Anticavity Tropical Mouth

ACT Total Care Sensitive Anticavity Tropical Mouth

Sodium Fluoride RINSE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41167-0969
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.09 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
sorbitol
Xylitol
POLOXAMER 407
BETAINE
propylene glycol
LEVOMENOL
CARNOSINE
GINGER
ANGELICA SINENSIS ROOT
LONICERA JAPONICA FLOWER
PUERARIA MONTANA VAR. LOBATA ROOT
POLYETHYLENE GLYCOL 600000
POLYETHYLENE GLYCOL 7000000
SODIUM BENZOATE
POTASSIUM SORBATE
sodium phosphate
POLYSORBATE 20
LACTIC ACID
edetate calcium disodium
cetylpyridinium chloride
FD&C RED NO. 40
D&C YELLOW NO. 10

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41167-0969-0 532 in 1 BOTTLE
2 NDC:41167-0969-3 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-01-01


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Be sure to consult your doctor before taking any medication!
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