DG Body Bar Soap Gold

Drug Labeling and Warnings

Drug Details [pdf]

BODY BAR GOLD- benzalkonium chloride soap 
Dolgencorp, LLC

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.

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DG Body Bar Soap Gold

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use

For washing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product

• avoid contact with the eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

• irritation or redness develops.

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, Water, Sodium Palm Kernelate, Glycerin, Zea Mays (Corn) Starch, Fragrance, Sodium Chloride, Sodium Laureth Sulfate, Etidronic Acid, Tetrasodium EDTA, FD&C Yellow No. 5, FD&C Red No. 4.

*This product is not manufactured or distributed by The Dial Corporation, a Henkel Company, owner of the registered trademark Dial®.

DISTRIBUTED BY DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

MADE IN COLUMBIA

100% Satisfaction Guaranteed

(888) 309-9030

DG body

BODY BAR SOAP GOLD

Antibacterial / Deodorant

• Gold formula protects from germs and odors
• Rich, creamy lather
• Clean-rinsing formula

Compare to active ingredient of Dial® Gold®

2 BARS

2-3.5 OZ SOAP BARS (99 g) TOTAL NET WT 7 OZ (198 g)

BODY BAR GOLD 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-202
Route of Administration	CUTANEOUS

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM PALMATE (UNII: S0A6004K3Z)
GLYCERIN (UNII: PDC6A3C0OX)
ETIDRONIC ACID (UNII: M2F465ROXU)
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	yellow	Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-202-11	2 in 1 BOX	10/27/2017	10/22/2019
1		99 g in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 55910-202-05	6 in 1 BOX	10/27/2017	10/22/2019
2		91 g in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/27/2017	10/22/2019

Labeler - Dolgencorp, LLC (068331990)

Revised: 10/2019

Document Id: 9586ae94-ef0b-3ec3-e053-2a95a90ac269

34390-5

Set id: 5c8bde5a-590d-085f-e053-2991aa0a56af

Version: 2

Effective Time: 20191022