STRETCH MARKS REMOVER STRETCH MARKS REMOVER- cocoa butter oil

Stretch Marks Remover by

Drug Labeling and Warnings

Stretch Marks Remover by is a Otc medication manufactured, distributed, or labeled by PHYTOPIA CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Cocoa butter (6%)

As skin protectant.

PURPOSE

Use

Helps to reduce stretch marks.

DOSAGE & ADMINISTRATION

Dosage Suggestion

Pregnant 6ml Maximum Per Day

Post-pragnant 6ml Maximum Per Day

INDICATIONS & USAGE

Directions

Apply on skin and gentlely massage around abdomen.

INACTIVE INGREDIENT

Other Ingredients

Rosa Canina Whole, Olive Oil, Citrus Aurantiifolia Leaf Oil, Citrus Aurantium Flower Oil, Evening Primrose Oil, Citrus Reticulata Fruit 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.

Stretch Marks Remover

Stretch Marks Remover

INGREDIENTS AND APPEARANCE

STRETCH MARKS REMOVER  STRETCH MARKS REMOVER
cocoa butter oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70470-1818
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COCOA BUTTER (UNII: 512OYT1CRR) (COCOA BUTTER - UNII:512OYT1CRR)	COCOA BUTTER	3.2 mg  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)	10.8 mL  in 50 mL
ROSA CANINA WHOLE (UNII: P5R39F12N2)
CITRUS AURANTIIFOLIA LEAF OIL (UNII: D8XVD1D0MQ)
CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
OLIVE OIL (UNII: 6UYK2W1W1E)

Product Characteristics
Color	purple (in 50ml miron glass bottle)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70470-1818-5	50 mL in 1 BOTTLE; 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 final	part346	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(70470-1818)