Label: BB BROAD SPECTRUM SPF 15 LIGHT TO MEDIUM- zinc oxide titanium dioxide cream
- NDC Code(s): 26052-031-01, 26052-031-02, 26052-031-03
- Packager: Burt's Bees
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- PURPOSE
- Uses
- Warnings
- Keep Out of Reach of Children
-
Directions
- Use in the morning after cleansing
- Apply liberally 15 minutes before sun exposure
- Children under 6 months: Ask a doctor
- Use a water resistent sunscreen if swimming or sweating
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early aging. To decrease this risk, regularly use a sunscreen with a broad spectrum spf of 15 or higher and other sun protection measures including:
- limit time in ethe sun, especially from 10 a.m.- 2 p.m.
- wear long-sleeve shirts, pants, hats and sunglasses
- reapply at least every 2 hours
- use a water resistent sunscreen if swimming or sweating
-
INACTIVE INGREDIENT
Inactive Ingredients: water, glycerin, decyl oleate, isoamyl cocoate, isoamyl laurate, octyldodecanol, polyglyceryl-4 caprate, caprylic/capric triglyceride, cetyl alcohol, helianthus annuus (sunflower) seed oil, polyglyceryl-2 dipolyhydroxystearate, glyceryl stearate citrate, stearic acid, morinda citrifilia fruit extract, beeswax, jojoba esters, mica, iron oxides, silica, sorbitan stearate, stearyl alcohol, behenyl alcohol, sodium carboxymethyl C10-16 alkyl glucoside, lauryl glucoside, magnesium aluminum silicate, xanthan gum, citric acid, isostearic acid, lecithin, polyglyceryl-3polyricinoleate, polyhydroxysteric acid, sodium phytate, trihydroxystearin, alumina, arachidyl alcohol, sorbic acid, alcohol denat., potassium sorbate, sodium benzoate, fragrance*, phenoxyehtanol
*natural fragrance
- Other Information:
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BB BROAD SPECTRUM SPF 15 LIGHT TO MEDIUM
zinc oxide titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:26052-031 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.7 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 7 g in 100 g Inactive Ingredients Ingredient Name Strength LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W) SODIUM BENZOATE (UNII: OJ245FE5EU) TRICAPRIN (UNII: O1PB8EU98M) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) OCTYLDODECANOL (UNII: 461N1O614Y) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) DOCOSANOL (UNII: 9G1OE216XY) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) DECYL OLEATE (UNII: ZGR06DO97T) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) JOJOBA OIL (UNII: 724GKU717M) ALUMINUM OXIDE (UNII: LMI26O6933) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) SORBIC ACID (UNII: X045WJ989B) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) CETYL ALCOHOL (UNII: 936JST6JCN) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) SUNFLOWER OIL (UNII: 3W1JG795YI) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) ISOSTEARIC ACID (UNII: X33R8U0062) ALCOHOL (UNII: 3K9958V90M) PHYTATE SODIUM (UNII: 88496G1ERL) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) YELLOW WAX (UNII: 2ZA36H0S2V) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) FERRIC OXIDE RED (UNII: 1K09F3G675) ISOAMYL LAURATE (UNII: M1SLX00M3M) STEARIC ACID (UNII: 4ELV7Z65AP) MORINDA CITRIFOLIA FRUIT (UNII: 7829X3G2X5) MICA (UNII: V8A1AW0880) ISOAMYL COCOATE (UNII: 14OG46E98E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:26052-031-01 1 in 1 CARTON 11/01/2015 1 NDC:26052-031-02 48.1 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:26052-031-03 0.85 g in 1 PACKET; Type 0: Not a Combination Product 11/01/2015 12/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/01/2015 Labeler - Burt's Bees (613480946)