STAY PUT SUNSCREEN SPF 30- octinoxate 7.50% octisalate 5.00% oxybenzone 4.00% homosalate 10.00% lotion

Stay Put Sunscreen SPF 30 by

Drug Labeling and Warnings

Stay Put Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by Sawyer Products Inc, Inspec Solution. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Actives                     Purpose

Octinoxate 7.50%       Sunscreen
Octisalate 5.00%        Sunscreen
Oxybenzone 4.00%    Sunscreen
Homosalate 10.00%   Sunscreen

PURPOSE

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

Directions

apply liberally to cool, dry skin
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 a long-sleeve shirts,
pants, hats, and sunglasses. children under 6
months: Ask a doctor

Warnings For external use only.

Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs

Keep out of reach of children

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

Inactive ingredeints

Purified Water
Hydrogenated Polyisobutene
Stearic Acid
Cetyl Alcohol
Amphisol (DEA-cetyl phosphate)
Glydant Plus Liquid
Triethanolamine
Carbopol 934
Acrylates/C10-30 Alkyl Crosspolymer
Aloe Barbadensis Leaf Juice
Hydrocloric Acid Reagent

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

STAY PUT SUNSCREEN SPF 30 
octinoxate 7.50% octisalate 5.00% oxybenzone 4.00% homosalate 10.00% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70392-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (BENZOPHENONE-3 - UNII:95OOS7VE0Y)	OXYBENZONE	4 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E)
STEARIC ACID (UNII: 4ELV7Z65AP)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHLORAMPHENICOL (UNII: 66974FR9Q1)
DMDM HYDANTOIN (UNII: BYR0546TOW)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) (UNII: K6MOM3T5YL)
ALOE (UNII: V5VD430YW9)
HYDROCHLORIC ACID (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70392-020-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/26/2026

Labeler - Sawyer Products Inc (118285923)

Registrant - Inspec Solution (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solution		081030372	manufacture(70392-020)