OTC Medication Information: ANTIBACTERIAL FOAMING

ANTIBACTERIAL FOAMING — triclosan liquid
KMART CORPORATION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient

Triclosan 0.46%


Purpose

Antibacterial

Uses

Helps reduce bacteria on the skin.

Warnings

For external use only.

When using this product

Avoid contact with eyes. If contact occurs, rinse with water.

Stop using this product and ask doctor if

Irritation or redness develops and lasts.

Keep out of reach of children

In case of accidental ingestion, get medical help and contact a Poison Control Center immediately.

Directions

Pump onto dry hands, work into a lather and rinse thoroughly.

Inactive Ingredients

WATER, SODIUM XYLENE SULFONATE, DIPROPYLENE GLYCOL, GLYCERIN, SODIUM PCA, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, POLYQUATERNIUM-10, FRAGRANCE, DISODIUM PHOSPHATE, CETYL ALCOHOL, ALOE BARBADENSIS LEAF JUICE, CITRIC ACID, METHYLPARABEN, PROPYLPARABEN, RED 4 (CI 14700), YELLOW 5 (CI 19140).

IMAGE OF ANTIBACTERIAL FOAMING
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ANTIBACTERIAL FOAMING
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49738-177
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (TRICLOSAN) TRICLOSAN 0.46 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
SODIUM XYLENESULFONATE
DIPROPYLENE GLYCOL
GLYCERIN
SODIUM PYRROLIDONE CARBOXYLATE
AMMONIUM LAURYL SULFATE
COCAMIDOPROPYL BETAINE
POLYQUATERNIUM-10 (400 CPS AT 2%)
SODIUM PHOSPHATE, DIBASIC, DIHYDRATE
CETYL ALCOHOL
ALOE VERA LEAF
CITRIC ACID MONOHYDRATE
METHYLPARABEN
PROPYLPARABEN
FD&C RED NO. 4
FD&C YELLOW NO. 5
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49738-177-08 221 mL in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 05/16/2011
Labeler — KMART CORPORATION (008965873)
Registrant — APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
Name Address ID/FEI Operations
APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture

Revised: 05/2011 KMART CORPORATION

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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