STRESS RELIEF HONZO SEIKA CHINESE HERBAL AROMA OIL- stress relief oil

Stress Relief by

Drug Labeling and Warnings

Stress Relief by is a Otc medication manufactured, distributed, or labeled by NIC CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Asian Ginseng 7mg

PURPOSE

Use

For treatment of headaches, emotional stress, sleep disorder and aniexty.

DOSAGE & ADMINISTRATION

Dosage Suggestion

Adults 5ml maximum per day

Children 1ml maximum per day

INACTIVE INGREDIENT

Other Ingredients

Bupleurum Chinense Root, Scutellaria Lateriflora, Lavender Oil, Bergamot Oil, Bitter Orange Oil, Sweet Cherry Oil, Walnut Oil, Jojoba Oil

INDICATIONS & USAGE

Directions

Apply on skin and gentle massage around affected area.

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

STRESS RELIEF   HONZO SEIKA CHINESE HERBAL AROMA OIL
stress relief oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71263-9901
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASIAN GINSENG (UNII: CUQ3A77YXI) (ASIAN GINSENG - UNII:CUQ3A77YXI)	ASIAN GINSENG	7 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SCUTELLARIA LATERIFLORA (UNII: 7BP4DH5PDC)
BITTER ORANGE OIL (UNII: 9TLV70SV6I)
SWEET CHERRY SEED OIL (UNII: 9X3RP3RJFH)
WALNUT OIL (UNII: Y0P3555R51)
JOJOBA OIL (UNII: 724GKU717M)
BERGAMOT OIL (UNII: 39W1PKE3JI)
LAVENDER OIL (UNII: ZBP1YXW0H8)
BUPLEURUM CHINENSE ROOT (UNII: BMA22623YK)

Product Characteristics
Color	brown (100ml per bottle)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71263-9901-1	100 mL 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
unapproved drug other		04/01/2016

Labeler - NIC CO., LTD. (690555759)

Registrant - NIC CO., LTD. (690555759)

Establishment
Name	Address	ID/FEI	Business Operations
NIC CO., LTD.		690555759	manufacture(71263-9901)