MENSTRUAL PAIN SYNERGY FOR TREATMENT OF MENSTRUAL PAIN- menstrual pain oil

Menstrual Pain Synergy by

Drug Labeling and Warnings

Menstrual Pain 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 0.6mg

Analgesic in the treatment of menstrual pain

PURPOSE

Use:

Menstrual Pain reliever

DOSAGE & ADMINISTRATION

Dosage Suggestion

Adults 4ml maximum per day

INDICATIONS & USAGE

Directions

Apply evenly to clean skin around lower abdomen. Simply apply 10~20 drops and rub into the skin. Apply twice a day. Can also use as a preventative by applying before menstrual.

INACTIVE INGREDIENT

Inactive Ingredients

Clary Sage Oil, Lavender Oil, Bergamot Oil, Olive Oil, Rose Hip Seed Oil, Evening Primrose 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.

MENSTRUAL PAIN Synergy

INGREDIENTS AND APPEARANCE

MENSTRUAL PAIN SYNERGY  FOR TREATMENT OF MENSTRUAL PAIN
menstrual pain oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70470-1805
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 mg  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
CLARY SAGE OIL (UNII: 87L0D4U3M0)
LAVENDER OIL (UNII: ZBP1YXW0H8)
BERGAMOT OIL (UNII: 39W1PKE3JI)
OLIVE OIL (UNII: 6UYK2W1W1E)
EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
ROSA RUBIGINOSA SEED OIL (UNII: 8M1P49MWAP)

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: 70470-1805-5	50 mL in 1 BOTTLE, UNIT-DOSE; 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(70470-1805)