Label: EQUATE SUNSCREEN TANNING OIL WITH COCONUT OIL SPF 6- avobenzone, homosalate spray
- NDC Code(s): 79903-085-80
- Packager: WAL-MART STORES INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 9, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and Ask a doctor if
- Keep out of reach of children.
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Directions
• Spray liberally and spread evenly by hand 15 minutes before sun exposure
• Hold can 4-6 inches away from the skin to apply
• Do not spray directly into face. Spray into hands then apply to face
• Do not apply in windy conditions
• Use in a well-ventilated area
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• children under 6 months of age: Ask a doctor - Other information
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Inactive ingredients
Mineral Oil, Ethylhexyl Palmitate, Diisopropyl Adipate, Isopropyl Myristate, Silica Dimethyl Silylate, Cocos Nucifera (Coconut) Oil, Fragrance, Theobroma Cacao (Cocoa) Seed Butter, Aloe Barbadensis Leaf Extract, PEG-8 Dimethicone, Plumeria Acutifolia Flower Extract, Mangifera Indica (Mango) Fruit Extract, Psidium Guajava Fruit Extract, Carica Papaya (Papaya) Fruit Extract, Passiflora Incarnata Fruit Extract, Colocasia Antiquorum Root Extract, Octyldodecanol, Retinyl Palmitate, Tocopheryl Acetate, Ascorbic Acid, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Hydrogenated Styrene/Butadiene Copolymer, Silica
- Label
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INGREDIENTS AND APPEARANCE
EQUATE SUNSCREEN TANNING OIL WITH COCONUT OIL SPF 6
avobenzone, homosalate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-085 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 40 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) COCONUT OIL (UNII: Q9L0O73W7L) ALOE VERA LEAF (UNII: ZY81Z83H0X) GUAVA (UNII: 74O70D6VG0) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H) PAPAYA (UNII: KU94FIY6JB) MANGO (UNII: I629I3NR86) PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P) PEG-8 DIMETHICONE (UNII: GIA7T764OD) OCTYLDODECANOL (UNII: 461N1O614Y) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) ASCORBIC ACID (UNII: PQ6CK8PD0R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) ETHYLHEXYL PALMITATE (UNII: 2865993309) SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) COCOA BUTTER (UNII: 512OYT1CRR) COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D) LIGHT MINERAL OIL (UNII: N6K5787QVP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-085-80 237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 11/15/2021 Labeler - WAL-MART STORES INC. (051957769)
