NDC | 59779-598-04, 59779-598-05 |
Set ID | 3df8005f-b26d-48fa-97bd-02fc9ac0275e |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS PHARMACY |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredients
- Use(s)
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure.
- Reapply at least every 2 hours.
- Use a water resistant sunscreen if swimming or sweating.
- Children under 6 months: Ask a doctor.
- Sun Protection Measure. 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 value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses.
- Other information
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Inactive ingredients
Water, C12-15 Alkyl Benzoate, Diethylhexyl 2,6-Naphthalate, Cetearyl Alcohol, Dimethicone, Cyclopentasiloxane, Glycerin, Cyclohexasiloxane, Arachidyl Alcohol, Phenyl Trimethicone, Phenoxyethanol, Cetearyl Glucoside, Panthenol, Benzyl Alcohol, Nylon-10/10, Chrysanthemum Parthenium (Feverfew) Extract, Behenyl Alcohol, Steareth-2, Sodium Cocoyl Amino Acids, Steareth-21, Fragrance, Polyacrylamide, Arachidyl Glucoside, Disodium EDTA, C13-14 Isoparaffin, Pentaerythrityl Tetra-di-t-Butyl Hydroxyhydrocinnamate, Sarcosine, Laureth-7, Ethylhexylglycerin, Iodopropynyl Butylcarbamate, Potassium Aspartate, Magnesium Aspartate.
- Questions or comments?
- Label Copy
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INGREDIENTS AND APPEARANCE
CVS PHARMACY CALMING DAILY MOISTURIZER
avobenzone, octinoxate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-598 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) PANTHENOL (UNII: WV9CM0O67Z) BENZYL ALCOHOL (UNII: LKG8494WBH) NYLON-12 (UNII: 446U8J075B) TANACETUM PARTHENIUM (UNII: 6GE7Z0761K) DOCOSANOL (UNII: 9G1OE216XY) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) EDETATE DISODIUM (UNII: 7FLD91C86K) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) SARCOSINE (UNII: Z711V88R5F) LAURETH-7 (UNII: Z95S6G8201) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) POTASSIUM ASPARTATE (UNII: OC4598NZEQ) MAGNESIUM ASPARTATE (UNII: R17X820ROL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-598-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:59779-598-05 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 11/16/2015 Labeler - CVS PHARMACY (062312574) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture(59779-598)