DR.ESLEE INTENSIVE RECOVERY BLEMISH BALM- zinc oxide cream

Dr.eslee Intensive Recovery Blemish Balm by

Drug Labeling and Warnings

Dr.eslee Intensive Recovery Blemish Balm by is a Otc medication manufactured, distributed, or labeled by Ajou Medics Co., Ltd, Ajou Medics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

zinc oxide

INACTIVE INGREDIENT

Water, Titanium Dioxide, Ethylhexyl Methoxycinnamate, Butylene Glycol, Hexyl Laurate, Caprylic/Capric Triglyceride, Cetyl Ethylhexanoate, Talc, Dipropylene Glycol, Dimethicone, Phenyl Trimethicone, Isoamyl p-Methoxycinnamate, Arbutin, Cetyl PEG/PPG-10/1 Dimethicone, Pentylene Glycol, 1,2-Hexanediol, Palmitoyl Pentapeptide-4, Copper Tripeptide-1, rh-Oligopeptide-1, Zinc Oxide, Magnesium Sulfate, Polyglyceryl-3 Diisostearate, Simmondsia Chinensis (Jojoba) Seed Oil, Sorbitan Olivate, Sorbitan Sesquioleate, Beeswax, Macadamia Ternifolia Seed Oil, Cyclopentasiloxane, Iron Oxides (CI 77492), Disteardimonium Hectorite, Aluminum Hydroxide, Iron Oxides (CI 77491), Triethoxycaprylylsilane, Iron Oxides (CI 77499), Tocopheryl Acetate, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Panthenol, Allantoin, Niacinamide, Adenosine, Bisabolol, Polysorbate 20, Aloe Barbadensis Leaf Juice, Centella Asiatica Extract, Snail Secretion Filtrate, Carbomer, Glycerin

PURPOSE

helps to protect from UV-Raysskin whitening and wrinkle removing

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply Proper Amount of the cream on skin

WARNINGS

■ For external use only.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.
■ Keep out of reach of children.
■ Stop use and ask doctor if rash and irritation develops.

DOSAGE & ADMINISTRATION

for topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.ESLEE INTENSIVE RECOVERY BLEMISH BALM 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76340-1301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.01248 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
OCTINOXATE (UNII: 4Y5P7MUD51)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76340-1301-1	60 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/23/2014

Labeler - Ajou Medics Co., Ltd (688796473)

Registrant - Ajou Medics Co., Ltd (688796473)

Establishment
Name	Address	ID/FEI	Business Operations
Ajou Medics Co., Ltd.		688796473	manufacture(76340-1301)