Label: VIVAIODAYS SUNSCREEN WITH TURMERIC- zinc oxide lotion
- NDC Code(s): 71778-001-01
- Packager: 5 SENCO 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 January 11, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
-
Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
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Directions
- apply liberally 15 minutes before sun exposure
- reapply:
- after 40 minutes of swimming or sweating
- immediately after towel drying
- 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 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-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
-
Inactive ingredients
SIMMONDSIA CHINENSIS (JOJOBA)SEED OIL 1, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL 1, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYROSPERMUM PARKII (SHEA) BUTTER 1, CERA ALBA/BEESWAX 1, HYDROGENATED VEGETABLE OIL, GLYCERYL STEARATE, OLEA EUROPAEA (OLIVE) FRUIT OIL 1, PARFUM, POLYHYDROXYSTEARIC ACID, HIPPOPHAE RHAMNOIDES (SEABUCKTHORN) FRUIT OIL 1, TOCOPHEROL, CURCUMA LONGA (TURMERIC) ROOT EXTRACT 1, CALENDULA OFFICINALIS (CALENDULA) FLOWER EXTRACT 1.
- 1
- From organic farming.
- Other information
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 100 ml Tube Label
-
INGREDIENTS AND APPEARANCE
VIVAIODAYS SUNSCREEN WITH TURMERIC
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71778-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength JOJOBA OIL (UNII: 724GKU717M) SUNFLOWER OIL (UNII: 3W1JG795YI) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) WHITE WAX (UNII: 7G1J5DA97F) SHEA BUTTER (UNII: K49155WL9Y) OLIVE OIL (UNII: 6UYK2W1W1E) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) TOCOPHEROL (UNII: R0ZB2556P8) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J) TURMERIC (UNII: 856YO1Z64F) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71778-001-01 100 mL in 1 TUBE; Type 0: Not a Combination Product 02/15/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/15/2018 12/31/2024 Labeler - 5 SENCO Inc. (055882668) Establishment Name Address ID/FEI Business Operations Stasinos Sikalias 363281305 manufacture(71778-001)
