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PHYLLIS GOLDEN HAIR ESSENCE

Dosage form: solution
Ingredients: OATMEAL 0.0008mL in 80mL
Labeler: UNOCOS CO., LTD.
NDC Code: 52841-020

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.

Drug Facts

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.

PHYLLIS GOLDEN  HAIR ESSENCE
oatmeal solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52841-020
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OATMEAL (OATMEAL) OATMEAL0.0008 mL  in 80 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
MUNG BEAN 
GOLD 
Packaging
#Item CodePackage Description
1NDC:52841-020-0180 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34704/01/2010
Labeler - UNOCOS CO., LTD. (557799050)
Registrant - UNOCOS CO., LTD. (557799050)
Establishment
NameAddressID/FEIOperations
UNOCOS CO., LTD.557799050manufacture

Revised: 01/2011
 
UNOCOS CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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