RENOKIN HAIR REVITALIZING description, usages, side effects, indications, overdosage, supplying and lots more!

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RENOKIN HAIR REVITALIZING

Caregen Co., Ltd.
Caregen Co., Ltd.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Active ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

Inactive ingredients:
Water (Aqua), Alcohol, Glycerin, Isopropyl Alcohol, Phenoxyethanol, Ginkgo Biloba Leaf Extract, Glycine Soja (Soybean) Oil, Hydrogenated Lecithin, Thuja Orientalis Extract, Disodium EDTA, Oligopeptide-54, Decapeptide-18, Serenoa Serrulata Fruit Extract, Polygala Tenuifolia Root Extract, Portulaca Oleracea Extract, Fragrance (Parfum), Decapeptide-10, Sodium Oleate, Retinyl Palmitate, Biotin

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warning:
For external use only, do not swallow.
In case of accidental ingestion, seek medical assistance.
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and consult a doctor if rash or irritation occurs.
Do not apply directly to a wound or open cut.
Keep out of reach of children.
Store at room temperature (below 25C).

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

Directions:
Apply the solution on dry scalp after using RENOKIN Hair Revitalizing Shampoo and Conditioner. Gently shake the solution before use. Spray to the target scalp area and lightly massage with fingertips. Do not wash off for 3 hours.
Use every morning and night.

DOSAGE AND ADMINISTRATION

Directions:
Apply the solution on dry scalp after using RENOKIN Hair Revitalizing Shampoo and Conditioner.
Gently shake the solution before use.
Spray to the target scalp area and lightly massage with fingertips.
Do not wash off for 3 hours.
Use every morning and night.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RENOKIN HAIR REVITALIZING

RENOKIN HAIR REVITALIZING

Allantoin SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60716-030
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALLANTOIN 0.3 mg

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60716-030-01 60 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2014-01-02


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Be sure to consult your doctor before taking any medication!
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