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NDC 69842-0148-27 CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

CVS Health is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE.

Product Information

NDC	69842-0148
Product ID	69842-148_c57651d5-30cb-52dd-e053-2995a90ae79b
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	CVS Health
Proprietary Name Suffix	SPF 70 Beach Guard Sun
Non-Proprietary Name	Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	30; 100; 50; 45; 40
Active Ingredient Units	mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Labeler Name	CVS Pharmacy
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 69842-0148-27 (69842014827)

Pricing Information	N/A
NDC Package Code	69842-148-27
Billing NDC	69842014827
Package	198 mL in 1 BOTTLE (69842-148-27)
Marketing Start Date	2014-10-03
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 4adbd66a-6b38-046d-e054-00144ff8d46c Details

Active ingredients

Avobenzone 3.0%, Homosalate 10.0%, Octisalate 5.0%, Octocrylene 4.5%, Oxybenzone 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

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 liberally 15 minutes before sun exposure

reapply:

• after 80 minutes of swimming or sweating

• immediately after towel drying

• at least every 2 hours

• children under 6 months: 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

Water, Styrene/Acrylates Copolymer, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Silica, Butyloctyl Salicylate, Dimethicone/PEG-10/15 Crosspolymer, Trisiloxane, Cetyl Dimethicone, Beeswax, Ethylhexylglycerin, Sodium Polyacrylate, Xanthan Gum, Ethylhexyl Stearate, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Behenyl Alcohol, Trideceth-6, Disodium EDTA, Glyceryl Stearate, PEG-100 Stearate, Caprylyl Glycol, Chlorphenesin, Fragrance, Propylene Glycol.

Labels

CVS HEALTH SPF 70 BEACH GUARD SUN LOTION BROAD SPECTRUM SPF 70 SUNSCREEN

6.7 FL OZ (198 mL)

NDC 69842-148-27

INGREDIENTS AND APPEARANCE

CVS HEALTH SPF 70 BEACH GUARD SUN

avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-148
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	45 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	40 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRISILOXANE (UNII: 9G1ZW13R0G)
DOCOSANOL (UNII: 9G1OE216XY)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)
WHITE WAX (UNII: 7G1J5DA97F)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CHLORPHENESIN (UNII: I670DAL4SZ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69842-148-27	198 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/03/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	10/03/2014

Labeler - CVS Pharmacy (062312574)

Revised: 6/2021

Document Id: c57651d5-30cb-52dd-e053-2995a90ae79b

Set id: 4adbd66a-6b38-046d-e054-00144ff8d46c

Version: 3

Effective Time: 20210623

Search by Drug Name or NDC

NDC 69842-0148-27 CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

Product Information

Package

Package Images

NDC 69842-0148-27 (69842014827)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 4adbd66a-6b38-046d-e054-00144ff8d46c Details

Active ingredients

Purpose

Uses

Warnings

Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

Directions

Other information

Inactive ingredients

Labels

INGREDIENTS AND APPEARANCE

Plavix (Clopidogrel) With Olive Oil Dosing Question

Can You Take A Z-Pak If You Have A Penicillin Allergy?

Search by Drug Name or NDC

NDC 69842-0148-27 CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Health 30; 100; 50; 45; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

Product Information

Package

Package Images

NDC 69842-0148-27 (69842014827)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 4adbd66a-6b38-046d-e054-00144ff8d46c Details

Active ingredients

Purpose

Uses

Warnings

Do not use

​When using this product​

​Stop use and ask a doctor if

Keep out of reach of children. ​

Directions

Other information

Inactive ingredients

Labels

INGREDIENTS AND APPEARANCE

When using this product

Stop use and ask a doctor if

Keep out of reach of children.