Studio Selection 950.000/950AA Sunscreen for Babies SPF 50

baby by

Drug Labeling and Warnings

baby by is a Otc medication manufactured, distributed, or labeled by Old East Main CO., Vi-Jon, LLC, Vi-Jon. LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BABY- sunscreen lotion 
Old East Main CO.

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Studio Selection 950.000/950AA
Sunscreen for Babies SPF 50

active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 4.5%

Octocrylene 8%

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

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 right away.

Directions

• apply liberaly 15 minutes before sun exposure
• apply to all skin exposed to the sun
• 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 rist, regularly use a sunscreen with Broad Spectrum SPF value 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-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect the product in this container from excessive heat and direct sun

inactive ingredients

water, glycerin, aluminum starch octenylsuccinate, styrene/acrylates copolymer, behenyl alcohol, glyceryl stearate, benzyl alcohol, PEG-100 stearate, polyester-7, tocopherol, arachidyl alcohol, acrylates/C10-30 alkyl acrylate crosspolymer, arachidyl glucoside, chlorphenesin, beeswax, silica, neopentyl glycol diheptanoate, potassium hydroxide, disodium EDTA

Disclaimers

*This product is not manufactured or distributed by Bayer distributor of Coppertone ®Sunscreen Lotion Water Babies Pure & Simple Broad Spectrum SPF 50.

May stain or damage some fabrics or surfaces

**Oxybenzone & Octinoxate Free

ADVERSE REACTION

DISTRIBUTED BY OLD EAST MAIN CO.

100 MISSION RIDGE, GOODLETTSVILLE, TN 37072

100% Satisfaction Guaranteed! (888)309-9030

REEF FRIENDLY**

Principal Panel Display

STUDIO SELECTION™

SUN

SUNSCREEN LOTION FOR BABIES

BROAD SPECTRUM SPF 50

Compare to Coppertone ®Water Babies Pure & Simple Broad Spectrum SPF 50*

• Water-Resistant (80 minutes)
• UVA/UVB Sunscreen

SPF 50

Pediatrician-Tested 

Hypoallergenic

8 FL OZ (236 mL)

BABY 
sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-937
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	450 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
DOCOSANOL (UNII: 9G1OE216XY)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYESTER-7 (UNII: 0841698D2F)
TOCOPHEROL (UNII: R0ZB2556P8)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
CHLORPHENESIN (UNII: I670DAL4SZ)
YELLOW WAX (UNII: 2ZA36H0S2V)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-937-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/13/2021	12/13/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/13/2021	12/13/2025

Labeler - Old East Main CO. (068331990)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(55910-937)

Revised: 12/2025

Document Id: 4617f904-716c-3968-e063-6294a90a83e2

34390-5

Set id: 6c87ca44-fcf8-46cc-8f05-336dc9315439

Version: 9

Effective Time: 20251216