Label: CARECELLA VELVET COVER BB CREAM- octinoxate, titanium dioxide, zinc oxide cream
- NDC Code(s): 69422-1003-1, 69422-1003-3
- Packager: General Bio Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 8, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Directions
-
Warnings
For external use only
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
Do not use when skin is red, inflamed, irritated, or painful
When using this product
do not apply on other parts of the body
do not use on damaged or broken skin
avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
do not apply directly to wound or open cut
Stop use and ask a doctor if
Rash or irritation on skin develops and lasts
-
Inactive Ingredients
Water, Cyclopentasiloxane, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Ethylhexyl Palmitate, Sorbitan Sesquioleate, Caprylic/Capric Triglyceride, Arbutin, Dimethicone, Dipropylene Glycol, CI 77492, Sodium Chloride, 1,2-Hexanediol, Beeswax,Disteardimonium Hectorite, Magnesium Aluminum Silicate,CI 77491, Hydroxyacetophenone,
Dimethicone/Vinyl Dimethicone Crosspolymer, CI 77499,PEG-10 Dimethicone Crosspolymer, Ozokerite,Aluminum Hydroxide, Triethoxycaprylylsilane, Lavandula Angustifolia (Lavender) Oil, Adenosine, Allantoin, Panthenol,
Chamomilla Recutita (Matricaria) Flower Extract,
Gentiana Lutea Root Extract, Artemisia Absinthium Extract, Portulaca Oleracea Extract, Acer Saccharum (Sugar Maple) Extract, Caprylyl Glycol.
- Uses
- Keep out of reach of children.
- Purpose
- Active Ingredient
- Carecella Velvet Cover BB Cream
-
INGREDIENTS AND APPEARANCE
CARECELLA VELVET COVER BB CREAM
octinoxate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69422-1003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 2.1 g in 50 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3.5 g in 50 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.75 g in 50 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69422-1003-3 1 in 1 BOX 05/10/2019 1 NDC:69422-1003-1 50 g in 1 TUBE; Type 0: Not a Combination Product 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/10/2019 Labeler - General Bio Co., Ltd. (695273863) Registrant - General Bio Co., Ltd. (695273863) Establishment Name Address ID/FEI Business Operations General Bio Co., Ltd. 695273863 manufacture(69422-1003)
