REMATEX- rematex pain relievingcream cream

Rematex by

Drug Labeling and Warnings

Rematex by is a Otc medication manufactured, distributed, or labeled by Home Aide Diagnostics, Inc., Zhejiang Bangli Medical Products Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS

Lidocain 4% --------------------------------------------------------------------------------------------------------- Topical analgesic
Menthol 1% --------------------------------------------------------------------------------------------------------- Topical analgesic

PURPOSE

PURPOSE

Topical analgesic

WARNINGS

WARNINGS

FOR EXTERNAL USE ONLY.

• When using this product use only as directed
• Do not bandage tightly
• Do not use with a heating pad
• Avoid contact with the eyes or mucous membranes
• Do not apply to wounds or damaged or irritated skin

DOSAGE & ADMINISTRATION

DIRECTIONS

Adults and children over 12 years

• Apply generously to affected area
• Massage into painful area until thoroughly absorbed into skin, repeat as necessary, not more than 3-4 times daily
• Store at 20°-25°C (68°-77 °F). Avoid direct sunlight.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

f swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

PREGNANCY OR BREAST FEEDING

If pregnant of breast-feeding, ask a healthcare professional before use

INACTIVE INGREDIENT

INACTIVE INGREDIENTS

aliphatic alcohol; stearic acid; vaseline; peregal; Carmellose Sodium; water;

INDICATIONS & USAGE

INDICATIONS

For the temporarily relieves minor pain associated with:

• Simple Backache
• Arthritis
• Strains
• Sprains
• Bruises

STOP USE

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 is present
• Irritation develops

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

REMATEX 
rematex pain relievingcream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69379-041
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69379-041-01	120 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/01/2015

Labeler - Home Aide Diagnostics, Inc. (783518983)

Registrant - Zhejiang Bangli Medical Products Co. Ltd (421295875)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Bangli Medical Products Co. Ltd		421295875	manufacture(69379-041)