Label: DOVE MEN PLUS CARE SENSITIVE FACE- avobenzone, ensulizole, octicsalate, octocrylene lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1333-1, 64942-1333-2, 64942-1333-3 - Packager: CONOPCO Inc. d/b/a Unilever
- 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 August 20, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions· apply liberally to face and neck 15 minutes before sun exposure
· reapply at least every 2 hours
· use a water resistant sunscreen if swimming or sweating
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 10a.m. - 2p.m.
· wear long-sleeved shirts, pants, hats, and sunglasses· children under 6 months of age; ask a doctor
- INACTIVE INGREDIENT
- QUESTIONS
- PDP 1.69 fl oz
- Carton 1.69 fl oz
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INGREDIENTS AND APPEARANCE
DOVE MEN PLUS CARE SENSITIVE FACE
avobenzone, ensulizole, octicsalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1333 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.0 g in 100 mL ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 1.5 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5.0 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 1.3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCOL STEARATE (UNII: 0324G66D0E) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONE (UNII: 92RU3N3Y1O) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POTASSIUM STEARATE (UNII: 17V812XK50) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETYL ALCOHOL (UNII: 936JST6JCN) XANTHAN GUM (UNII: TTV12P4NEE) STEARAMIDE AMP (UNII: U3K8640346) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1333-2 1 in 1 CARTON 1 NDC:64942-1333-1 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:64942-1333-3 15 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 not final part352 01/12/2016 Labeler - CONOPCO Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Unilever Manufacturing (US), Inc. 021679448 manufacture(64942-1333)