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Bullfrog Surfer

Dosage form: gel
Ingredients: OCTINOXATE 0.075g in 1mL, OCTOCRYLENE 0.1g in 1mL, OXYBENZONE 0.03g in 1mL
Labeler: Chattem, Inc.
NDC Code: 41167-3301

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

BullFrog Surfer Gel

Drug Facts

Active ingredients

Octinoxate 7.5%

Octocrylene 10%

Oxybenzone 3%

Purpose

Sunscreens

Uses
  • higher SPF gives more sunburn protection
  • helps prevent sunburn

Warnings

For external use only

When using this product
  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if
  • rash or irritation develops and lasts

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • apply liberally before sun exposure and as needed
  • reapply after prolonged swimming, vigorous activity or towel drying
  • children under 6 months: ask a doctor

Inactive ingredients

aloe barbadensis leaf extract, beeswax, caprylic/capric triglyceride, cyclomethicone, fragrance, isopropyl myristate, isopropyl palmitate, isostearyl alcohol, silica, tocopheryl acetate (245-136)

PRINCIPAL DISPLAY PANEL

Bull Frog® 
SPF 36
Surfer FormulaTM 
Gel Sunblock
8 Hour Waterproof
UVA/UVB Protection
Sweatproof
Original Amphibious Formula
5 FL OZ (147 ML)

BULLFROG SURFER 
octinoxate and octocrylene and oxybenzone gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-3301
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE0.075 g  in 1 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE0.1 g  in 1 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE0.03 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
YELLOW WAX 
CYCLOMETHICONE 
ISOPROPYL MYRISTATE 
ISOPROPYL PALMITATE 
ISOSTEARYL ALCOHOL 
SILICON DIOXIDE 
.ALPHA.-TOCOPHEROL ACETATE, D- 
Packaging
#Item CodePackage Description
1NDC:41167-3301-7147 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35201/01/1989
Labeler - Chattem, Inc. (003336013)
Establishment
NameAddressID/FEIOperations
Chattem Plant 1003336013MANUFACTURE, PACK

Revised: 05/2011
Document Id: 53e525b8-5faf-4139-bd4c-4b5f6ac808db
Set id: 5983136e-5dcd-40d8-878b-cf34d82c3482
Version: 2
Effective Time: 20110521
 
Chattem, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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