Label: NIVEA MEN SENSITIVE PROTECTIVE- avobenzone, octisalate, octocrylene lotion
- NDC Code(s): 10356-575-16
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
-
DOSAGE & ADMINISTRATION
Directions
For sunscreen use:
• apply liberally 15 minutes before sun exposure
• use a water resistant sunscreen if swimming or sweating
• 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 of age: Ask a doctor -
INACTIVE INGREDIENT
Inactive ingredients
Water, Isopropyl Palmitate,Glycerin, Tapioca Starch, Cetearyl
Alcohol, Glyceryl Stearate Citrate, Tocopheryl Acetate, Panthenol,
Chamomilla Recutita (Matricaria) Flower Extract, Hamamelis
Virginiana (Witch HazeL) Bark/Leaf Extract, 1,2-Hexanediol, Carbomer,
Ethylhexylglycerin, Maltodextrin, Caprylic/Capric Triglyceride,
Acrylates/Cl0-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide,
Trisodium EDTA, Phenoxyethanol, Piroctone OIamine, Fragrance.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NIVEA MEN SENSITIVE PROTECTIVE
avobenzone, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-575 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.7 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 8.4 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) GLYCERIN (UNII: PDC6A3C0OX) STARCH, TAPIOCA (UNII: 24SC3U704I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) PANTHENOL (UNII: WV9CM0O67Z) CHAMOMILE (UNII: FGL3685T2X) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) HEXANEDIOL (UNII: ZIA319275I) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MALTODEXTRIN (UNII: 7CVR7L4A2D) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE TRISODIUM (UNII: 420IP921MB) PHENOXYETHANOL (UNII: HIE492ZZ3T) PIROCTONE OLAMINE (UNII: A4V5C6R9FB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-575-16 75 mL in 1 TUBE; Type 0: Not a Combination Product 09/15/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/15/2014 Labeler - Beiersdorf Inc (001177906)
