NATURAL SENSE SPF 50 SUNSCREEN- sunscreen cloth

Natural Sense SPF 50 Sunscreen by

Drug Labeling and Warnings

Natural Sense SPF 50 Sunscreen by is a Otc medication manufactured, distributed, or labeled by Dr. Natural LLC, Jell Pharma. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Sunscreen

ACTIVE INGREDIENT

Active ingredients
Octinoxate 5% .................................. Sunscreen
Octisalate 3% .................................. Sunscreen
Avobenzone 3% .................................. Sunscreen
Octocrylene 6% ................................ Sunscreen

WHEN USING

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

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DO NOT USE

Do not use on damaged or broken skin.

INDICATIONS & USAGE

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.

DOSAGE & ADMINISTRATION

Apply liberally and evenly 15 minutes before sun exposure.
Reapply at least every 2 hours.
Use a water resistant sunscreen if swimming or sweating.
Children under 6 months of age: ask a doctor.

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 swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Water, Glycerin, Phenoxyethanol, Ethylhexylglycerin, Polyacrylate-13,
Polyisobutene, Polysorbate 20, Fragrance, Aloe Barbadensis Leaf Extract,
Camellia Sinensis Leaf Extract, Tocopherol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATURAL SENSE SPF 50 SUNSCREEN 
sunscreen cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78261-324
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	6 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
FRAGRANCE 13576 (UNII: 5EM498GW35)
CAMELLIA SINENSIS LEAF OIL (UNII: VC855RRT77)
GLYCERIN (UNII: PDC6A3C0OX)
VITAMIN E POLYETHYLENE GLYCOL SUCCINATE (UNII: O03S90U1F2)
POLYACRYLATE-13 (UNII: FS2D4T67EA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78261-324-09	25 g in 1 PACKET; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	01/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/01/2026

Labeler - Dr. Natural LLC (080454165)

Establishment
Name	Address	ID/FEI	Business Operations
Jell Pharma		726025211	manufacture(78261-324)