Label: RENOVE UV SHIELD BROAD SPECTRUM SPF 50- avobenzone, octinoxate sunscreen cream
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Contains inactivated NDC Code(s)
NDC Code(s): 60782-003-00 - Packager: Y.S. Health Corp.
- 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 March 7, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- ACTIVE INGREDIENTS
- USES
- WARNINGS
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DIRECTIONS
- Apply liberally 15 minutes before sun exposure.
- Reapply after 80 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 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 years of age: Ask a doctor.
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INACTIVE INGREDIENTS
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES
DICAPRYLYL CARBONATE
FRAGARIA VESCA FRUITGLYCERIN
SUNFLOWER SEED
WATER
CAPRYLHYDROXAMIC ACID
CAPRYLYL GLYCOL1,2-HEXANEDIOL
LINSEED OIL
EVENING PRIMROSE OIL
CHIA SEED OIL
ACAI OIL
TRISODIUM ETHYLENEDIAMINE DISUCCINATE
XANTHAN GUM
AMARANTHUS CAUDATUS SEED
VACHELLIA FARNESIANA WHOLE
ORANGE
GREEN TEA LEAFAcrylates
Plankton Extract
- OTHER INFORMATION
- Product Label
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INGREDIENTS AND APPEARANCE
RENOVE UV SHIELD BROAD SPECTRUM SPF 50
avobenzone, octinoxate sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60782-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6.2 g in 10 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 10 mL Inactive Ingredients Ingredient Name Strength ORANGE (UNII: 5EVU04N5QU) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU) GLYCERIN (UNII: PDC6A3C0OX) SUNFLOWER SEED (UNII: R9N3379M4Z) WATER (UNII: 059QF0KO0R) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) LINSEED OIL (UNII: 84XB4DV00W) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) CHIA SEED OIL (UNII: MC2LH51BO7) ACAI OIL (UNII: Z0W6766A2W) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) XANTHAN GUM (UNII: TTV12P4NEE) AMARANTHUS CAUDATUS SEED (UNII: FJ722PPQ9M) VACHELLIA FARNESIANA WHOLE (UNII: YPI49T6HNL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60782-003-00 2 in 1 BOX 03/10/2017 1 50 mL in 1 CONTAINER; 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 08/04/2015 Labeler - Y.S. Health Corp. (612982504) Registrant - Y.S. Health Corp. (612982504)