LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40

LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40 by

Drug Labeling and Warnings

LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40 by is a Otc medication manufactured, distributed, or labeled by Salt and Stone LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40- zinc oxide cream 
Salt and Stone LLC

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LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40

Drug Facts

Active Ingredients

Zinc Oxide (Non-Nano) 22.75%

Purpose

Sunscreen

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

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 immediately.

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 10am - 2pm.
• Wear long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months: Ask a doctor

Other Information

• Protect this product from excess heat and direct sun.

Inactive Ingredients

Purified Water, Coco-Caprylate/Caprate, Caprylic/Capric Triglyceride, Octyldodecanol, Glycerol, Cetearyl Alcohol, Polyglyceryl-3 Polyricinoleate, Hyaluronic Acid, PEG-30 Dipolyhydroxystearate, Gluconolactone, Isostearic Acid, Sodium Chloride, Cetearyl Glucoside, Xanthan Gum, EDTA, Sodium Benzoate.

Package Labeling:

LIGHTWEIGHT SHEER DAILY SUNSCREEN SPF 40 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71585-140
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	227.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
OCTYLDODECANOL (UNII: 461N1O614Y)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
HYALURONIC ACID (UNII: S270N0TRQY)
PEG-30 DIPOLYHYDROXYSTEARATE (4000 MW) (UNII: 9713Q0S7FO)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
ISOSTEARIC ACID (UNII: X33R8U0062)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
XANTHAN GUM (UNII: TTV12P4NEE)
EDETIC ACID (UNII: 9G34HU7RV0)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71585-140-00	60 mL in 1 TUBE; Type 0: Not a Combination Product	06/01/2021	07/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/01/2021	07/01/2023

Labeler - Salt and Stone LLC (080683697)

Revised: 10/2023

Document Id: 07fdf946-b7aa-de3f-e063-6394a90a709d

34390-5

Set id: c29bda99-480d-3244-e053-2a95a90ae502

Version: 2

Effective Time: 20231018