OTC Medication Information: PHYLLIS GOLDEN HAIR ESSENCE

PHYLLIS GOLDEN HAIR ESSENCE- oatmeal solution
UNOCOS CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient: OATMEAL

Inactive Ingredients:

WATER, LAMINARIA DIGITATA EXTRACT, HYDROXYETHYLCELLULOSE, NONOXYNOL-12, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, BAMBUSA ARUNDINACEA STEM EXTRACT, PHASEOLUS RADIATUS SEED EXTRACT, GOLD, METHYLCHLOROISOTHIAZOLINONE, FRAGRANCE

Purpose:

It appears to protect the cuticle layers of the damage hair, and it seems to make glossy and healthy hair by reinforcing the immunity of the hair root.

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, sensitivity, and etc., caused by direct sunlight.
Do not use the products on sun burnt, wounded, eczema or dermatitis-affected regions.
If the product gets into your eyes, rinse your eyes with clean water.
Caution rinse thoroughly. Can cause loss of hair or discoloration.

Keep out of reach of children:
Replace the caps after use.
Keep away from babies and children.

How to Use:

Apply to wet or damp hair and scalp with soft massage after hair drying.

Dosage and Administration:

Apply to wet or damp hair and scalp with soft massage after hair drying.

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PHYLLIS GOLDEN HAIR ESSENCE
oatmeal solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:52841-020
Route of Administration CUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OATMEAL (OATMEAL) OATMEAL 0.0008 mL in 80 mL
Inactive Ingredients
Ingredient Name Strength
WATER
MUNG BEAN
GOLD
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52841-020-01 80 mL in 1 CARTON None
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 Operations
UNOCOS CO., LTD. 557799050 manufacture

Revised: 01/2011 UNOCOS CO., LTD.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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