Next1 TM Anti-bacterial Deodorant Sport Bar

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses for washing to decrease bacteria on the skin

Warnings

For external use only

When using this product do not use in or near the eyes, in case of eye contact, flush with water

Stop use and ask a doctor if irritation or redness develop

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Wet bar with water.
Lather vigorously and wash skin.
Rinse and dry thoroughly.

Inactive ingredients Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Chloride, Sodium Lauryl Sulfate, Fragrance, Titanium Dioxide, Coconut Acid, Citric Acid, Etidronic Acid, Tetrasodium EDTA, Green 3, Red 33. May contain Caramel.

Distributed by:

Olivette Products, L.L.C.

Bridgeton, MO 63044

Phone: 1-800-325-8998

MADE IN COLOMBIA

Kills germs
Odor protection

Next 1 TM

Anti-bacterial

Deodorant

Sport Bar

Contains no animal fat

NET WT 5 OZ (142g)

label

NEXT1 ANTI-BACTERIAL DEODORANT SPORT
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51870-003
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM PALMATE (UNII: S0A6004K3Z)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
GLYCERIN (UNII: PDC6A3C0OX)
CARAMEL (UNII: T9D99G2B1R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
COCONUT ACID (UNII: 40U37V505D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETIDRONIC ACID (UNII: M2F465ROXU)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51870-003-05	142 g in 1 BOX; Type 0: Not a Combination Product	06/15/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	06/15/2017

Labeler - Keefe Group (839439601)