Search by Drug Name or NDC

NDC 41163-0951-64 Equaline Kids Continuous Sunscreen SPF 50 30; 100; 50; 40; 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

Equaline Kids Continuous Sunscreen SPF 50 30; 100; 50; 40; 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

Equaline Kids Continuous Sunscreen SPF 50 is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by SUPERVALU INC.. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.

Product Information

NDC	41163-0951
Product ID	41163-951_d61b7442-a7f9-62c4-e053-2a95a90ad9b4
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Equaline Kids Continuous Sunscreen SPF 50
Proprietary Name Suffix	n/a
Non-Proprietary Name	Homosalate, Octisalate, Oxybenzone, Octocrylene, Avobenzone
Product Type	HUMAN OTC DRUG
Dosage Form	SPRAY
Route	TOPICAL
Active Ingredient Strength	30; 100; 50; 40; 50
Active Ingredient Units	mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Labeler Name	SUPERVALU INC.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part352
Listing Certified Through	2024-12-31

Package

Package Images

NDC 41163-0951-64 (41163095164)

Pricing Information	N/A
NDC Package Code	41163-951-64
Billing NDC	41163095164
Package	2 CAN in 1 PACKAGE (41163-951-64) / 207 mL in 1 CAN (41163-951-86)
Marketing Start Date	2011-12-21
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL d61b7098-31c3-3b30-e053-2a95a90a2d39 Details

Active Ingredients

Avobenzone 3.0%,

Homosalate 10.0%,

Octisalate 5.0%,

Octocrylene 4.0%,

Oxybenzone 5.0%

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

FLAMMABLE

do not use near heat, flame or while smoking
avoid long term storage above 104 deg F (40 degC)

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.
Do not puncture or incinerate. Contents under pressure.
Do not store at temperatures above 120 deg F.

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 liberally 15 minutes before sun exposure
Hold can 4-6 inches away form body, spray evenly to ensure complete coverage
Do not spray into face. Spray into hand and apply to face.
Use in well ventilated, but not windy areas

Reapply:
After 80 minutes of swimming or sweating
Immdiately after towel drying
At least every 2 hours

Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease theis 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 10 am - 2 pm
wear long sleeved shirts, pants, hats, and sunglasses

children under 6 months: Ask a doctor

Inactive Ingredients

Alcohol denat. (73.2% v/v), acrylates/octylacrylamide copolymer, stearoxytrimethylsilane, glycerin, diethylhexyl syringylidene malonate, tocopherol (vitamin E), fragrance, retinyl palmitate (vitamin A palmitate), caprylic/capric triglyceride

Other information

protect the product in this container from excessive heat and direct sun
may stain or damage some fabrics, materials or surfaces

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUALINE KIDS CONTINUOUS SUNSCREEN SPF 50

homosalate, octisalate, oxybenzone, octocrylene, avobenzone spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41163-951
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	40 mg in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	50 mg in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)
GLYCERIN (UNII: PDC6A3C0OX)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
TOCOPHEROL (UNII: R0ZB2556P8)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:41163-951-64	2 in 1 PACKAGE	12/21/2011
1	NDC:41163-951-86	207 mL in 1 CAN; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	12/21/2011

Labeler - SUPERVALU INC. (006961411)

Revised: 1/2022

Document Id: d61b7442-a7f9-62c4-e053-2a95a90ad9b4

Set id: d61b7098-31c3-3b30-e053-2a95a90a2d39

Version: 1

Effective Time: 20220121