TENDINITICA SYNERGY FOR TREATMENT OF TENDINITIS- tendinitica oil

Tendinitica Synergy by

Drug Labeling and Warnings

Tendinitica Synergy by is a Otc medication manufactured, distributed, or labeled by PHYTOPIA CO., LTD., Phytopia Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

menthol(2.6%)

Balsam Peru Oil (2.4%)

Analgesic in the treatment of muscle pain

PURPOSE

Use

Helps relieve the condition of pain and stiffness.

DOSAGE & ADMINISTRATION

Dosage Suggestion

Adults 5ml maximum per day

Children 1ml maximum per day

INDICATIONS & USAGE

Directions

Apply on skin and gentle massage around painful area.

INACTIVE INGREDIENT

Inactive Ingredients

EUCALYPTUS RADIATA LEAF OIL, JAVA CITRONELLA OIL, SUNFLOWER OIL, JOJOBA OIL, ROSEMARY OIL, EVENING PRIMROSE OIL, LEMON OIL, LAVENDER OIL

KEEP OUT OF REACH OF CHILDREN

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children.

STORAGE AND HANDLING

Other Information

Protect this product from excessive heat

and direct sun.

WARNINGS

Warnings

For external use only. Stop use and ask doctor if rash occurs. Keep out reach of children.

PainAway-With natural Peppermint and Balsam Peru Oil

INGREDIENTS AND APPEARANCE

TENDINITICA SYNERGY  FOR TREATMENT OF TENDINITIS
tendinitica oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70470-1139
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.3 mg  in 50 mg

Inactive Ingredients
Ingredient Name	Strength
MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
CLARY SAGE OIL (UNII: 87L0D4U3M0)
LAVENDER OIL (UNII: ZBP1YXW0H8)
OLIVE OIL (UNII: 6UYK2W1W1E)
SUNFLOWER OIL (UNII: 3W1JG795YI)
JOJOBA OIL (UNII: 724GKU717M)
ROSEMARY OIL (UNII: 8LGU7VM393)
BERGAMOT OIL (UNII: 39W1PKE3JI)

Product Characteristics
Color	brown (50ml per bottle)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70470-1139-5	500 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	04/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	04/01/2016

Labeler - PHYTOPIA CO., LTD. (656940504)

Registrant - PHYTOPIA CO., LTD. (656940504)

Establishment
Name	Address	ID/FEI	Business Operations
Phytopia Co., Ltd.		656940504	manufacture(70470-1139)