PHYLLIS GOLDEN HAIR- oatmeal shampoo

PHYLLIS GOLDEN by

Drug Labeling and Warnings

PHYLLIS GOLDEN by is a Otc medication manufactured, distributed, or labeled by UNOCOS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: OATMEAL

INACTIVE INGREDIENT

Inactive Ingredients:

WATER, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, PEG-7 GLYCERYL COCOATE, GLYCINE, SOJA (SOYBEAN) SEED EXTRACT, DECYL SODIUM CHLORIDE,
POLYQUATERNIUM-10, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, BAMBUSA ARUNDINACEA STEM EXTRACT,
PHASEOLUS RADIATUS SEED EXTRACT, LAMINARIA DIGITATA EXTRACT, GOLD, CITRIC ACID, BENZOPHENONE-5, DISODIUM EDTA, METHYLISOTHIAZOLINONE,
METHYLCHLOROISOTHIAZOLINONE, FRAGRANCE

PURPOSE

Purpose:

It appears to protect from harmful ultraviolet rays as well as preventing oxidation.
Alleviates skin trouble from sensitive scalp while making glossy healthy hair.

WARNINGS

WARNINGS:

Use of the products should be discontinued if the following adverse reactions occur. As continued use may make symptoms worse, it is advisable to consult a dermatologist, Redness, swelling, itching, and sensitivity.
    Redness, swelling, itching, and sensitivity caused by direct sunlight.
Do not use the products on sun burnt areas, wounded, eczema or dermatitis-affected regions.
If the product gets into your eyes, rinse your eyes with clean water.
Caution rinse thoroughly. If not, may cause loss of hair or discoloration

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

Replace the caps after use.

Keep away from babies and children.

INDICATIONS & USAGE

How to Use:

Apply to wet or damp hair with soft massage and rinse thoroughly.

DOSAGE & ADMINISTRATION

Dosage and administration:

Apply to wet or damp hair with soft massage and rinse thoroughly.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHYLLIS GOLDEN  HAIR
oatmeal shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52841-010
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y)	OATMEAL	0.004 mL  in 400 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCINE (UNII: TE7660XO1C)
GOLD (UNII: 79Y1949PYO)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52841-010-01	400 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	04/01/2010

Labeler - UNOCOS CO., LTD. (557799050)

Registrant - UNOCOS CO., LTD. (557799050)

Establishment
Name	Address	ID/FEI	Business Operations
UNOCOS CO., LTD.		557799050	manufacture