Label: BB BROAD SPECTRUM SPF 15 MEDIUM- zinc oxide titanium dioxide cream
- NDC Code(s): 26052-032-01, 26052-032-02
- Packager: Burt's Bees
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 5, 2023
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- Official Label (Printer Friendly)
- Active Ingredients
- PURPOSE
- INDICATIONS & USAGE
- Warnings
- Keep out of reach of children.
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Directions
- Use in the morning after cleansing
- Apply liberally 15 minutes before sun exposure
- Children under 6 months: Ask a doctor
- 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 of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. to 2 p.m.
- wear long sleeve shirts, pants, hats and sunglasses
- reapply at least every two hours
- use a water resistant sunscreen if swimming or sweating
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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 citrifolia 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, xanthum gum, citric acid, isostearic acid, lecithin, polyglyceryl-3 polyrincinoleate, polyhydroxystearic acid, sodium phytate, trihydroxystearin, alumina, arachidyl alcohol, sorbic acid, alcohol denat., potassium sorbate, sodium benzoate, fragrance, phenoxyethanol
- Other Information
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BB BROAD SPECTRUM SPF 15 MEDIUM
zinc oxide titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:26052-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 7 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.7 g in 100 g Inactive Ingredients Ingredient Name Strength DOCOSANOL (UNII: 9G1OE216XY) JOJOBA OIL (UNII: 724GKU717M) ALCOHOL (UNII: 3K9958V90M) ISOSTEARIC ACID (UNII: X33R8U0062) FERRIC OXIDE RED (UNII: 1K09F3G675) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) ALUMINUM OXIDE (UNII: LMI26O6933) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DECYL OLEATE (UNII: ZGR06DO97T) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) CETYL ALCOHOL (UNII: 936JST6JCN) YELLOW WAX (UNII: 2ZA36H0S2V) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRICAPRIN (UNII: O1PB8EU98M) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) OCTYLDODECANOL (UNII: 461N1O614Y) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) SUNFLOWER OIL (UNII: 3W1JG795YI) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) SODIUM BENZOATE (UNII: OJ245FE5EU) PHYTATE SODIUM (UNII: 88496G1ERL) ISOAMYL COCOATE (UNII: 14OG46E98E) SORBIC ACID (UNII: X045WJ989B) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ISOAMYL LAURATE (UNII: M1SLX00M3M) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) STEARIC ACID (UNII: 4ELV7Z65AP) MORINDA CITRIFOLIA FRUIT (UNII: 7829X3G2X5) MICA (UNII: V8A1AW0880) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:26052-032-02 1 in 1 CARTON 11/01/2015 1 NDC:26052-032-01 48.1 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 11/01/2015 Labeler - Burt's Bees (613480946)