Label: NO BS SPF20 MOISTURIZER- octinoxate, avobenzone, octocrylene cream
- NDC Code(s): 71852-060-50
- Packager: Product Management LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings:
-
Directions:
- Apply liberally 15 minutes before sun exposure.
- Reapply:
- At least every two hours.
- Immediately after swimming, sweating, or towel drying.
SUN PROTECTION MEASURES:
Spending time in the sun increases your risk of skin cancer abnd early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including:
- Limit time in the sun, especially between 10am and 2pm.
- Wear long sleeve shirts, pants, hats and sunglasses.
- For children under six months, consult a physician.
-
Inactive Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Beeswax, Bis-Vinyl Dimethicone/Dimethicone Copolymer, C18-38 Alkyl Hydroxystearoyl Stearate, Calendula Officinalis Extract, Caprylyl Glycol, Carbomer, Cyclopentasiloxane, Glycerin, Glyceryl Stearate, Isodecyl Neopentanoate, Isohexadecane, Lavandula Angustifolia (Lavender) Oil, PEG-100 Stearate, Phenoxyethanol, Plantain Extract, Polysorbate-80, Rosmarinus Officinalis (Rosemary) Extract, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Tetrasodium EDTA.
- OTHER INFORMATION:
- Packaeg
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INGREDIENTS AND APPEARANCE
NO BS SPF20 MOISTURIZER
octinoxate, avobenzone, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71852-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 55 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) YELLOW WAX (UNII: 2ZA36H0S2V) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) ISOHEXADECANE (UNII: 918X1OUF1E) LAVENDER OIL (UNII: ZBP1YXW0H8) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ROSEMARY (UNII: IJ67X351P9) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71852-060-50 1 in 1 CARTON 11/01/2017 1 50 mL 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 11/01/2017 Labeler - Product Management LLC (080906171)
