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NDC 69842-0146-27 CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

CVS Pharmacy 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	69842-0146
Product ID	69842-146_ecacbcfa-a637-f23c-e053-2a95a90a810e
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 Pharmacy
Proprietary Name Suffix	SPF 30 Beach Guard Sun
Non-Proprietary Name	Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	27; 80; 50; 35; 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 69842-0146-27 (69842014627)

Pricing Information	N/A
NDC Package Code	69842-146-27
Billing NDC	69842014627
Package	198 mL in 1 BOTTLE (69842-146-27)
Marketing Start Date	2017-03-16
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 4ad94400-5f89-6e34-e054-00144ff8d46c Details

Active ingredients

Avobenzone 2.7%, Homosalate 8.0%, Octisalate 5.0%, Octocrylene 3.5%, 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

• 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

• children under 6 months: Ask a doctor

Other information

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

• may stain or damage some fabrics, materials or surfaces

Inactive ingredients

Water, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Butyloctyl Salicylate, Acrylates/C12-22 Alklmethacrylate Copolymer, Caprylyl Glycol, Silica, Cetyl Dimethicone, Beeswax, PPG-12/SMDI Copolymer, Ethylhexylglycerin, Dimethicone/PEG-10/15 Crosspolymer, Trilsiloxane, Ethylhexyl Stearate, Behenyl Alcohol, Sodium Polyacrylate, Trideceth-6, Styrene/Acrylates Copolymer, Disodium EDTA, Glyceryl Stearate, PEG-100 Stearate, Xanthan Gum, Chlorphenesin, Fragrance.

Label

INGREDIENTS AND APPEARANCE

CVS PHARMACY SPF 30 BEACH GUARD SUN

avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-146
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	35 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	80 mg in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	27 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)
POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)
TRISILOXANE (UNII: 9G1ZW13R0G)
DOCOSANOL (UNII: 9G1OE216XY)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)
YELLOW WAX (UNII: 2ZA36H0S2V)
PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
PEG-100 STEARATE (UNII: YD01N1999R)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CHLORPHENESIN (UNII: I670DAL4SZ)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69842-146-27	198 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/16/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	03/16/2017

Labeler - CVS Pharmacy (062312574)

Revised: 11/2022

Document Id: ecacbcfa-a637-f23c-e053-2a95a90a810e

Set id: 4ad94400-5f89-6e34-e054-00144ff8d46c

Version: 5

Effective Time: 20221104

Search by Drug Name or NDC

NDC 69842-0146-27 CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

Product Information

Package

Package Images

NDC 69842-0146-27 (69842014627)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 4ad94400-5f89-6e34-e054-00144ff8d46c Details

Active ingredients

Purpose

Uses

Warnings

Do not use

When using this product

Stop use and ask a doctor

Keep out of reach of children.

Directions

Other information

Inactive ingredients

Label

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 69842-0146-27 CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

CVS Pharmacy 27; 80; 50; 35; 40 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

Product Information

Package

Package Images

NDC 69842-0146-27 (69842014627)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 4ad94400-5f89-6e34-e054-00144ff8d46c Details

Active ingredients

Purpose

Uses

Warnings

​Do not use ​​

​When using this product​

​Stop use and ask a doctor

​Keep out of reach of children.

Directions

Other information

Inactive ingredients

Label

INGREDIENTS AND APPEARANCE

Do not use

When using this product

Stop use and ask a doctor

Keep out of reach of children.