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NDC 49035-0843-39 Equate SUNSCREEN spf 50 SPORT 30; 100; 50; 40 mg/g; mg/g; mg/g; mg/g Details

Equate SUNSCREEN spf 50 SPORT 30; 100; 50; 40 mg/g; mg/g; mg/g; mg/g

Equate SUNSCREEN spf 50 SPORT is a TOPICAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Walmart. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE.

Product Information

NDC	49035-0843
Product ID	49035-843_ec39eb1f-22cc-6b32-e053-2995a90aef1b
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	Equate SUNSCREEN spf 50 SPORT
Proprietary Name Suffix	broadspectrum
Non-Proprietary Name	Avobenzone,Homosalate,Octisalate,Octocrylene
Product Type	HUMAN OTC DRUG
Dosage Form	SPRAY
Route	TOPICAL
Active Ingredient Strength	30; 100; 50; 40
Active Ingredient Units	mg/g; mg/g; mg/g; mg/g
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Labeler Name	Walmart
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 49035-0843-39 (49035084339)

Pricing Information	N/A
NDC Package Code	49035-843-39
Billing NDC	49035084339
Package	312 g in 1 CAN (49035-843-39)
Marketing Start Date	2019-01-29
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 4e5280b2-1437-4d97-bb4c-db1a1632fea7 Details

Active ingredients

Avobenzone 3.0%

Homosalate 10.0%

Octisalate 5.0%

Octocrylene 4.0%

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°F (40°C)

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove. • Keep away from face to avoid breathing it. • do not puncture or incinerate. Contents under pressure. • do not store at temperatures above 120° F.

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.

Directions

• Spray liberally and spread evenly by hand 15 minutes before sun exposure

• Hold can 4-6 inches away from the skin to apply

• Do not spray directly into face. Spray into hands then apply to face

• Do not apply in windy conditions

• Use in a well-ventilated area

• reapply:

• after 80 minutes of swimming or sweating

• immediately after towel drying

• at least every 2 hours

• children under 6 months of age: Ask a doctor

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 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

Other information

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

• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

alcohol denat., butyloctyl salicylate, acrylates/octylacrylamide copolymer, panthenol, tocopherol, fragrance, stearoxytrimethylsilane,

caprylic/capric triglyceride, glycerin

Label

INGREDIENTS AND APPEARANCE

EQUATE SUNSCREEN SPF 50 SPORT BROADSPECTRUM

avobenzone,homosalate,octisalate,octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-843
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)
PANTHENOL (UNII: WV9CM0O67Z)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-843-48	258 g in 1 CAN; Type 0: Not a Combination Product	01/29/2019
2	NDC:49035-843-39	312 g in 1 CAN; Type 0: Not a Combination Product	01/29/2019
3	NDC:49035-843-63	2 in 1 PACKAGE	01/29/2019
3	NDC:49035-843-37	156 g in 1 CAN; Type 0: Not a Combination Product
4	NDC:49035-843-75	624 g in 1 CAN; Type 0: Not a Combination Product	01/29/2019	12/02/2019
5	NDC:49035-843-78	516 g in 1 CAN; Type 0: Not a Combination Product	01/29/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/29/2019

Labeler - Walmart (051957769)

Revised: 10/2022

Document Id: ec39eb1f-22cc-6b32-e053-2995a90aef1b

Set id: 4e5280b2-1437-4d97-bb4c-db1a1632fea7

Version: 7

Effective Time: 20221030