NDC | 71909-1220-0, 71909-1220-1 |
Set ID | 5f7a9b43-c77f-3822-e053-2a91aa0a042b |
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
Chamaecyparis Obtusa Leaf Extract, Cyclopentasiloxane, Butylene Glycol, Silica,
Cyclohexasiloxane, Niacinamide, 1,2-Hexanediol, Cetyl PEG/PPG-10/1 Dimethicone,
Sorbitan Sesquioleate, PEG-10 Dimethicone, Hexyl Laurate, Sodium Chloride, Ozokerite,
Caprylic/Capric Triglyceride, Stearic Acid, Alumina, Xanthan Gum, Methicone,
Triethoxycaprylylsilane, Lavandula Angustifolia (Lavender) Extract, Rosmarinus Officinalis
(Rosemary) Extract, Origanum Vulgare Flower/Leaf/Stem Extract, Thymus Vulgaris
(Thyme) Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Fragrance,
Iron Oxide Yellow(CI 77492), Ethylhexylglycerin,Adenosine, Iron Oxide Red (CI 77491) - OTC-ASK ODCTOR SECTION
- OTC - DO NOT USE SECTION
- OTC - KEEP OUT OF REACH OF CHILDREN SECTION
-
WARNINGS SECTION
Warnings
*For external use only
*Do not use on damaged or broken skin
*When using this product keep our 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 - Dosage & administration section
- M Suit Sun Block SPF50+ PA+++
-
INGREDIENTS AND APPEARANCE
LOVLUV M SUIT SUN BLOCK
titanium dioxide, octinoxate,zinc oxide, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71909-1220 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 2.5 g in 50 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 2 g in 50 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2 g in 50 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 1 g in 50 g Inactive Ingredients Ingredient Name Strength CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB) 23.1555 g in 50 g Product Characteristics Color yellow Score no score Shape ROUND Size 125mm Flavor BERRY Imprint Code 120mm Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71909-1220-1 1 in 1 BOX 01/31/2018 12/31/2018 1 NDC:71909-1220-0 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(71909-1220)