GOLD BOND MEDICATED ORIGINAL STRENGTH BODY- menthol powder

Gold Bond Medicated Original Strength Body by

Drug Labeling and Warnings

Gold Bond Medicated Original Strength Body by is a Otc medication manufactured, distributed, or labeled by Gold Bond Co LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Gold Bond Medicated

Original Strength Body Powder

Drug Facts

Active ingredient

Menthol 0.15%

Purpose

Anti-itch

Uses

temporarily relieves the pain and itch associated with:

■ minor cuts  ■ sunburn  ■ insect bites  ■ scrapes ■ minor burns ■ minor skin irritations   

Warnings

For external use only

When using this product

■ avoid contact with eyes

Stop use and ask a doctor if

■ condition worsens

■ symptoms persist for more than 7 days or clear up and occur again within a few days

■ redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

■ adults and children 2 years and older: apply freely up to 3 or 4 times daily  

■ children under 2 years: ask a doctor

■ for best results dry skin thoroughly before applying

Inactive ingredients

zea mays (corn) starch, zinc oxide, acacia senegal gum, silica, tricalcium phosphate, eucalyptol, methyl salicylate, salicylic acid, zinc stearate, thymol

PRINCIPAL DISPLAY PANEL

GOLD BOND
ORIGINAL STRENGTH
BODY POWDER

Net wt 10 oz (283 g)

PRINCIPAL DISPLAY PANEL

GOLD BOND
MEDICATED
ORIGINAL STRENGTH
BODY POWDER
Net wt 1 OZ (28 g)

INGREDIENTS AND APPEARANCE

GOLD BOND MEDICATED ORIGINAL STRENGTH BODY 
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84714-0110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
ZINC OXIDE (UNII: SOI2LOH54Z)
ACACIA (UNII: 5C5403N26O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
EUCALYPTOL (UNII: RV6J6604TK)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
ZINC STEARATE (UNII: H92E6QA4FV)
THYMOL (UNII: 3J50XA376E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84714-0110-9	283 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021
2	NDC: 84714-0110-6	113 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021
3	NDC: 84714-0110-0	28 g in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2021

Labeler - Gold Bond Co LLC (119184861)