NDC | 71909-0780-0, 71909-0780-1 |
Set ID | 5f8d08bd-1406-5416-e053-2a91aa0a3a35 |
Category | HUMAN OTC DRUG LABEL |
Packager | Cnt Dream. Co., Ltd |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- OTC - ACTIVE INGREDIENT SECTION
-
INACTIVE INGREDIENT SECTION
Camellia Japonica Flower Water,Cyclopentasiloxane,Caprylic/Capric Triglyceride,
Cyclohexasiloxane,Glycerin,Cyclomethicone,Arbutin,1,2-Hexanediol,
Cetyl PEG/PPG-10/1 Dimethicone,Sorbitan Sesquioleate,Beeswax,PEG-10 Dimethicone,
Sodium Chloride,Iron Oxide Yellow (CI 77492),Ozokerite,Magnesium Aluminum Silicate,
Iron Oxide Red (CI 77491),Methicone,Triethoxycaprylylsilane,Iron Oxide Black (CI 77499),
Melaleuca Alternifolia (Tea Tree) Leaf Water,Centella Asiatica Extract,Chamomilla
Recutita (Matricaria) Flower Extract,Glycyrrhiza Glabra (Licorice) Root Extract,
Camellia Sinensis Leaf Extract,Polygonum Cuspidatum Root Extract,Rosmarinus
Officinalis (Rosemary) Leaf Extract,Scutellaria Baicalensis Root Extract,Butylene Glycol,
Alcohol,Fragrance,Ethylhexylglycerin,Adenosine - OTC - ASK DOCTOR SECTION
- OTC - DO NOT USE SECTION
- OTC - -KEEP OUT OF REACH OF CHILDREN SECTION
-
WARNINGS SECTION
*For external use only
*Do not use on damaged or broken skin
*When using this product keep out of eyes, Rinse with water to remove.
*Stop use and ask a doctor if rash or irritation develops and lasts.
*Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away - OTC- PURPOSE SECTION
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INDICATIONS & USAGE SECTION
Uses
*helps prevent sunburn
*if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sunDirections:
Apply a proper amount evenly for the last step of skin care.
For sunscreen use:
*apply liberally 15 minutes before sun exposure
*reapply at least every 2 hours
*use a water resistant sunscreen if swimming or sweating
* Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
*limit time in the sun, especially from 10a.m-2p.m
*wear long-sleeved shirts, pants, hats, and sunglasses
*children under 6 months of age: Ask a doctor - PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LOVLUV VIVACITY BRIGHT BB CREAM
titanium dioxide, octinoxate, zinc oxide, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71909-0780 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3.5 g in 50 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 2 g in 50 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.65 g in 50 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 2.5 g in 50 g Inactive Ingredients Ingredient Name Strength CAMELLIA JAPONICA FLOWER OIL (UNII: 5CXP06X16D) 22.815 g in 50 g CYCLOMETHICONE 6 (UNII: XHK3U310BA) 2.35 g in 50 g Product Characteristics Color brown Score no score Shape ROUND Size 150mm Flavor BERRY Imprint Code 150;a Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71909-0780-1 1 in 1 BOX 01/31/2018 12/31/2018 1 NDC:71909-0780-0 50 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/31/2018 Labeler - Cnt Dream. Co., Ltd (694699750) Registrant - Cnt Dream. Co., Ltd (694699750) Establishment Name Address ID/FEI Business Operations Cnt Dream. Co., Ltd 694699750 manufacture(71909-0780)