OTC Medication Information: J and R Perfect Essence Beblesh Balm (40mL)

J AND R PERFECT ESSENCE BEBLESH BALM (40ML) — titanium dioxide and octinoxate cream
WIZCOZ CORPORATION 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.

Label1
Box Label
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Ingredients:

Water, Cyclopentasiloxane, Titatinum Dioxide, Butylene Glycol, Ethylhexyl Methoxycinnamate, Cyclohexasiloxane, 4-Methylbenzylidene Camphor, Glycerin, Silica, Lauryl PEG/PPG-18/18 Methicone, Arbutin, Sodium Chloride, Dimethicone, Hydrogenated Polydecene, Octyldodecyl Myristate, Phenyl Trimethicone, Sorbitan Olivate, Dimethicone/Vinyl Dimethicone Crosspolymer, Beeswax, Ozokerite, Sorbitan Sesquioleate, CI 11492, Hexyl Laurate, Disteardimonium Hectorite, Butylene Glycol Dicaprylate/Dicaprate, Lecithin, Triethoxycaprylylsilane, CI 77499, Dimethiconol, CI 77491, Portulaca Oleracea Extract, PEG/PPG-19/19 Dimethicone, Methylparaben, Calcium Stearate, Chlorphenesin, Propylene Carbonate, Chamomilla Recutita (Matricaria) Flower Extract, Propylene Glycol Stearate, Butylparaben, Fragrance, Polysorbate 20, Sorbitan Laurate, Propylene Glycol Laurate, Disodium EDTA, Rosmarinus Officinalis (Rosemary) Leaf Extract, Angelica Keiskei Leaf/Stem Extract, Panax Ginseng Root Extract, Oryza Sativa (Rice) Extract, Lentinus Edodes Extract

DIRECTIONS: Use it proper quantity on the area of your face like patting at the last step of skin care.

J AND R PERFECT ESSENCE BEBLESH BALM (40ML)
titanium dioxide octinoxate cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49715-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TITANIUM DIOXIDE (TITANIUM) TITANIUM DIOXIDE 3.6 mL in 40 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE 1.6 mL in 40 mL
Product Characteristics
Color brown (Brown) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49715-001-02 40 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part352 12/01/2009
Labeler — WIZCOZ CORPORATION LTD (690397273)
Registrant — WIZCOZ CORPORATION LTD (690397273)
Establishment
Name Address ID/FEI Operations
WIZCOZ CORPORATION LTD 690397273 manufacture

Revised: 11/2009 WIZCOZ CORPORATION 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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