SUNSCREEN SPF 30 DAYLOGIC

Main information

  • Trade name:
  • SUNSCREEN SPF 30 DAYLOGIC- avobenzone 2.00% homosalate 10.50% octisalate 5.00% octocrylene 2.00% oxybenzone 2.00% lotion
  • Composition:
  • Avobenzone 2 mg in 100 mL
  • Administration route:
  • TOPICAL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • SUNSCREEN SPF 30 DAYLOGIC- avobenzone 2.00% homosalate 10.50% octisalate 5.00% octocrylene 2.00% oxybenzone 2.00% lotion
    United States
  • Language:
  • English

Therapeutic information

  • Therapeutic indications:
  • Uses • helps prevent sunburn

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • OTC monograph not final
  • Authorization number:
  • 11822-1113-6, 11822-1113-9
  • Last update:
  • 22-06-2019

Summary of Product characteristics: dosage, interactions, side effects

SUNSCREEN SPF 30 DAYLOGIC- avobenzone 2.00% homosalate 10.50% octisalate 5.00%

octocrylene 2.00% oxybenzone 2.00% lotion

Rite Aid

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 Facts

Active ingredients Purpose

Avobenzone 2.00%.Sunscreen

Homosalate 10.50%.Sunscreen

Octisalate 5.00%.Sunscreen

Octocrylene 2.00%.Sunscreen

Oxybenzone 2.00%.Sunscreen

Uses helps prevent sunburn

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical

help or contact a Poison Control Center right away

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 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

Aloe Barbadensis Leaf Juice

Barium Sulfate

Benzyl Alcohol

Carbomer

Cocos Nucifera (Coconut) Oil

Dimethicone

Disodium EDTA

Fragrance

Methylparaben

Mineral Oil

Neopentyl Glycol Diheptanoate

Polyester-7

Polyglyceryl-3 Distearate

Propylparaben

Simmondsia Chinensis (Jojoba) Oil

Sorbitan Isostearate

Sorbitol

Stearic Acid

Tocopherol

Triethanolamine

VP/Eicosene Copolymer

Water

SUNSCREEN SPF 30 DAYLOGIC

avobenzone 2.00% homosalate 10.50% octisalate 5.00% octocrylene 2.00% oxybenzone 2.00% lotion

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:118 22-1113

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

Avo benzo ne (UNII: G6 3QQF2NOX) (AVOBENZONE - UNII:G6 3QQF2NOX)

Avo be nz o ne

2 mg in 10 0 mL

Ho mo sa la te (UNII: V0 6 SV4M9 5S) (HOMOSALATE - UNII:V0 6 SV4M9 5S)

Ho mo sa la te

10 .5 mg in 10 0 mL

O ctisa la te (UNII: 4X49 Y0 59 6 W) (OCTISALATE - UNII:4X49 Y0 59 6 W)

O c tisa la te

5 mg in 10 0 mL

O cto crylene (UNII: 5A6 8 WGF6 WM) (OCTOCRYLENE - UNII:5A6 8 WGF6 WM)

O c to c ryle ne

2 mg in 10 0 mL

O xybenzo ne (UNII: 9 5OOS7VE0 Y) (OXYBENZONE - UNII:9 5OOS7VE0 Y)

O xybe nz o ne

2 mg in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)

Ba rium Sulfa te (UNII: 25BB7EKE2E)

Benzyl Alco ho l (UNII: LKG8 49 4WBH)

CARBO MER 9 4 0 (UNII: 4Q9 3RCW27E)

CO CO NUT O IL (UNII: Q9 L0 O73W7L)

Dimethico ne (UNII: 9 2RU3N3Y1O)

EDETATE DISO DIUM (UNII: 7FLD9 1C8 6 K)

Methylpa ra ben (UNII: A2I8 C7HI9 T)

Minera l O il (UNII: T5L8 T28 FGP)

Neo pentyl Glyco l Dihepta no a te (UNII: 5LKW3C543X)

Po lyester-7 (UNII: 0 8 416 9 8 D2F)

Po lyg lyceryl-3 Distea ra te (UNII: ZI1LK470 XV)

Pro pylpa ra ben (UNII: Z8 IX2SC1OH)

JO JO BA O IL (UNII: 724GKU717M)

So rbita n Iso stea ra te (UNII: 0 1S2G2C1E4)

So rbito l (UNII: 50 6 T6 0 A25R)

Stea ric Acid (UNII: 4ELV7Z6 5AP)

To co phero l (UNII: R0 ZB2556 P8 )

TRO LAMINE (UNII: 9 O3K9 3S3TK)

VINYLPYRRO LIDO NE/EICO SENE CO PO LYMER (UNII: 0 35MV9 S1C3)

Wa ter (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:118 22-1113-6

236 mL in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 16

2

NDC:118 22-1113-9

473 mL in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

11/30 /20 16

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt352

11/30 /20 16

Labeler -

Rite Aid (014578892)

Registrant -

Product Quest Mfg (927768135)

Establishment

Rite Aid

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Pro duct Quest Mfg

9 2776 8 135

manufacture(118 22-1113) , label(118 22-1113)

Revised: 5/2018