SYNC PRO- sync relief pro cream cream

SYNC PRO by

Drug Labeling and Warnings

SYNC PRO by is a Otc medication manufactured, distributed, or labeled by iON Pharma, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts active ingredients

Active ingredients: Purpose

Methyl salicylate 30%: Topical Analgesic

Menthol 10%: Topical Analgesic

Camphor 4%: Topical Analgesic

Uses

Uses Temporarily relieves the minor aches and pains of muscles and joints associated

with:

• simple backache
• arthritis
• strains
• bruises
• sprains

Do not use section

Do not use

• on wounds or damaged skin
• with a heating pad
• on a child under 12 years of age with arthritis-like conditions

When using this product section

When using this product

• avoid contact with eyes or mucous membranes
• do not bandage tightly

Stop use section

Stop use and ask a doctor if

• condition worsens or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation occurs

Keep out of reach of children section

Keep out of reach of children

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

Directions section

Directions

• use only as directed
• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
• children under 12 years of age: ask a doctor

INACTIVE INGREDIENT

Inactive ingredients

Carbomer, Disodium EDTA, Glyceryl Stearate, Lanolin, Polysorbate 80, Potassium Hydroxide, Stearic Acid, Water

Questions or comments section

Questions or comments:

833.711.8833

info@syncrelief.com

PRINCIPAL DISPLAY PANEL

NDC: 82944-400-10

syn relief PRO

Relief in Motion

LONG LASTING RELIEF

PAIN RELIEF CREAM
Topical Analgesic

Light Scent

NET WT 4 oz (113 g)

FOR EXTERNAL USE ONLY

INGREDIENTS AND APPEARANCE

SYNC PRO 
sync relief pro cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82944-400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	30 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
STEARIC ACID (UNII: 4ELV7Z65AP)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
LANOLIN (UNII: 7EV65EAW6H)
CARBOMER (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
GLYCERYL STEARATE (UNII: 230OU9XXE4)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82944-400-10	1 in 1 BOX	04/01/2025
1		113 in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2025

Labeler - iON Pharma, LLC (118739596)