MY MEDIC SUNSCREEN SPF 30- ethylhexyl methoxycinnamate, octocrylene, homosalate, butyl methoxy dibenzoyl methane and titanium dioxide gel

My Medic by

Drug Labeling and Warnings

My Medic by is a Otc medication manufactured, distributed, or labeled by Sled Distribution, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyhexyl Methoxycinnamate 7.0%

Octocrylene 6.0%

Homosalate 5.0%

Butyl Methoxy Dibenzoyl Methane 2.5%

Titanium Dioxide 1.0%

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 right away.

Directions

• Apply to skin liberally, avoiding the eye area.
• Wait at least 30 mins before sun exposure, or as directed by a physician.
• Re-apply after 80 mniutes of swimming and/or sweating.
• re-apply immediately after towel drying and at least every 3 hours.

Inactive ingredients

Water, Caprylic/Capric Triglyceride, Isopropyl Mynstate, Beeswax, Glyceryl Stearate, Butyloctyl Salicylate, VP/Eicosene Copolymer, Steareth-20, PEG-100 Stearate, Steareth-2, Xanthan Gum, Aloe, Barbadensis Leaf Extract, Sodium Benzoate, Sodium Hyaluronate, Potassium Sorbate, Disodium EDTA.

Other information

• Protect the product in this container from excessive heat and direct sunlight.

SUNSCREEN

INGREDIENTS AND APPEARANCE

MY MEDIC  SUNSCREEN SPF 30
ethylhexyl methoxycinnamate, octocrylene, homosalate, butyl methoxy dibenzoyl methane and titanium dioxide gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81417-125
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.07 g  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.06 g  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	0.05 g  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.01 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
STEARETH-20 (UNII: L0Q8IK9E08)
PEG-100 STEARATE (UNII: YD01N1999R)
STEARETH-2 (UNII: V56DFE46J5)
XANTHAN GUM (UNII: TTV12P4NEE)
ALOE (UNII: V5VD430YW9)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81417-125-01	3.5 g in 1 BAG; Type 0: Not a Combination Product	03/24/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	03/24/2022

Labeler - Sled Distribution, LLC (079772888)

Registrant - Sled Distribution, LLC (079772888)

Establishment
Name	Address	ID/FEI	Business Operations
Sled Distribution, LLC		079772888	manufacture(81417-125)