Label: SEEME BEAUTY MOISTURIZER WITH SUNSCREEN SPF 30- avobenzone, homosalate, octocrylene, octyl salicylate lotion
- NDC Code(s): 69423-560-10, 69423-560-50
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 16, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- PURPOSE
- Uses
-
DOSAGE & ADMINISTRATION
• Apply liberally 15 minutes before sun exposure.
• Reapply at least every 2 hours
• 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 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.• children under 6 months: ask doctor
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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Inactive Ingredients
Water
Tapioca Starch
Glycerin
Niacinamide
Persea Gratissima (Avocado) Oil
Dimethicone
Cetearyl Alcohol
Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Butylene Glycol
Isohexadecane
Butyrospermum Parkii (Shea) Butter
Curcuma Longa (Turmeric) Root Extract
Caprylyl Glycol
1,2-Hexanediol
Phenoxyethanol
Tocopheryl Acetate
Dimethiconol
PEG-100 Stearate
Polysorbate 60
Cetearyl Glucoside
Polymethylsilsesquioxane
Sorbitan Isostearate
Disodium EDTA
Peucedanum Graveolens (Dill) Extract
Stearic Acid
Palmitic Acid
Xanthan Gum
Cynara Scolymus (Artichoke) Leaf Extract
Lavandula Angustifolia (Lavender) Oil
Citrus Limon (Lemon) Peel Oil
- Other information
- Questions or comments?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SEEME BEAUTY MOISTURIZER WITH SUNSCREEN SPF 30
avobenzone, homosalate, octocrylene, octyl salicylate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-560 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONOL GUM (UNII: 4MJ9GU3T1P) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) ISOHEXADECANE (UNII: 918X1OUF1E) LAURIC ACID (UNII: 1160N9NU9U) STARCH, TAPIOCA (UNII: 24SC3U704I) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ARACHIDIC ACID (UNII: PQB8MJD4RB) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) TURMERIC (UNII: 856YO1Z64F) LEMON OIL (UNII: I9GRO824LL) CYNARA SCOLYMUS LEAF (UNII: B71UA545DE) LAVENDER OIL (UNII: ZBP1YXW0H8) MYRISTIC ACID (UNII: 0I3V7S25AW) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) POLYSORBATE 60 (UNII: CAL22UVI4M) NIACINAMIDE (UNII: 25X51I8RD4) PALMITIC ACID (UNII: 2V16EO95H1) PEG-100 STEARATE (UNII: YD01N1999R) AVOCADO OIL (UNII: 6VNO72PFC1) DILL (UNII: Y05PC4JZRH) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-560-10 1 in 1 BOX 07/06/2021 1 10 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69423-560-50 1 in 1 BOX 07/06/2021 2 50 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 not final part352 07/06/2021 Labeler - The Procter & Gamble Manufacturing Company (004238200)