DailyMed - WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

NDC Code(s): 71782-115-01, 71782-601-01
Packager: DUKE CANNON SUPPLY CO.

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None

Drug Label Information

Updated April 29, 2025

If you are a consumer or patient please visit this version.

Download DRUG LABEL INFO: PDF XML
Official Label (Printer Friendly)

View All Sections

SPL UNCLASSIFIED SECTION
Drug Facts

Drug Facts
Close
ACTIVE INGREDIENT
Active ingredients Pupose - Avobenzone 2%Sunscreen - Octinoxate 6.5%Sunscreen - Octisalate 5%Sunscreen - Octocylene 1.5%Sunscreen

Active ingredients Pupose

Avobenzone 2% Sunscreen

Octinoxate 6.5% Sunscreen

Octisalate 5% Sunscreen

Octocylene 1.5% Sunscreen

Close
Uses
helps prevent sunburn

helps prevent sunburn
Close
WARNINGS
Warnings - Do not use - on damaged or broken skin - When using this product - keep out of eyes - Stop use and ask a doctor if - rash occurs - Keep out of reach of children

Warnings

Do not use

on damaged or broken skin

When using this product

keep out of eyes

Stop use and ask a doctor if

rash occurs

Keep out of reach of children

Close
Directions
apply liberally 15 minutes before sun exposure - reapply at least every 2 house - use a water-resistant sunscreen if swimming or sweating - Sun protection meaures: spending time in the sun ...
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 house
- use a water-resistant sunscreen if swimming or sweating
- Sun protection meaures: 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 value of 15 or higher and other sun protection measures including:
  - limit time int he sun, especailly from 10 a.m.-2 p.m.
  - wear long-sleeved shirts, pants, hats, and sunglasses
  - children under 6 months of age: ask a doctor
Close
Other Information
protect this product from excessive heat and direct sun.

protect this product from excessive heat and direct sun.
Close
Inactive ingredients
organic sunflower oil, organic beeswax, organic coconut oil, organic shea butter, peppermint oil, natural flavor, organic tamanu oil, organic matcha tea, tocopherol, organic calendula extract ...

organic sunflower oil, organic beeswax, organic coconut oil, organic shea butter, peppermint oil, natural flavor, organic tamanu oil, organic matcha tea, tocopherol, organic calendula extract, organic stevia
Close
Questions or comments?
call 1.855.354.4438 www.dukecannon.com

call 1.855.354.4438 www.dukecannon.com
Close
Tube Package
DUKE - CANNON - SUPPLY CO. CANNON BALM - OFFENSIVELY LARGE SUNSCREEN LIP BALM - HYDRATE+DEFEND - SPF 15 BROAD SPECTRUM SPF 15 - TACTICAL SUNSCREEN - Formulated to meet the needs of U.S. Military personnel - MADE ...

DUKE

CANNON

SUPPLY CO.

CANNON BALM

OFFENSIVELY LARGE SUNSCREEN LIP BALM

HYDRATE+DEFEND

SPF 15 BROAD SPECTRUM SPF 15

TACTICAL SUNSCREEN

Formulated to meet the needs of U.S. Military personnel

MADE IN USA

with imported ingredients.

Net Wt 0.56 oz (17g)

Dist. by Duke Cannon Supply Co.

Minneapolis, MN 55401

Peel here for drug facts

Close
PRINCIPAL DISPLAY PANEL
DUKE CANNON SUPPLY CO. Winter Rescue Kit - Survival Tools for Hands and Lips

DUKE CANNON SUPPLY CO.

Winter Rescue Kit

Survival Tools for Hands and Lips

Close

INGREDIENTS AND APPEARANCE

Product Information

WINTER RESCUE KIT octinoxate, octisalate, octocrylene, avobenzone kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71782-601

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71782-601-01	1 in 1 CARTON	11/01/2024

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 TUBE	17 g
Part 2	3 JAR	127.5 g

Part 1 of 2

CANNON BALM octinoxate, octisalate, octocrylene, avobenzone stick

Product Information
Item Code (Source)	NDC:71782-115
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.255 g in 17 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.34 g in 17 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.105 g in 17 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.85 g in 17 g

Ingredient Name	Strength
Inactive Ingredients
SUNFLOWER OIL (UNII: 3W1JG795YI)
YELLOW WAX (UNII: 2ZA36H0S2V)
COCONUT OIL (UNII: Q9L0O73W7L)
SHEA BUTTER (UNII: K49155WL9Y)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
PEPPERMINT OIL (UNII: AV092KU4JH)
TAMANU OIL (UNII: JT3LVK84A1)
TOCOPHEROL (UNII: R0ZB2556P8)

Product Characteristics
Color		Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71782-115-01	17 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	05/07/2021

Part 2 of 2

BLOODY KNUCKLES HAND REPAIR BALM body and hand (excluding shaving preparations), leave-on [skin care preparations (creams, lotions, powder, and sprays)] lotion

Product Information
Route of Administration	TOPICAL

Ingredient Kind	Ingredient Name	Quantity
Other Ingredients
INGR	MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
INGR	TRIBEHENIN (UNII: 8OC9U7TQZ0)
INGR	JOJOBA OIL (UNII: 724GKU717M)
INGR	TOCOPHEROL (UNII: R0ZB2556P8)
INGR	LANOLIN (UNII: 7EV65EAW6H)
INGR	SHEA BUTTER (UNII: K49155WL9Y)
INGR	GLYCERIN (UNII: PDC6A3C0OX)
INGR	STEARIC ACID (UNII: 4ELV7Z65AP)
INGR	WHITE WAX (UNII: 7G1J5DA97F)
INGR	CETYL ALCOHOL (UNII: 936JST6JCN)
INGR	DIMETHICONE (UNII: 92RU3N3Y1O)
INGR	ALLANTOIN (UNII: 344S277G0Z)
INGR	ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
INGR	PHENOXYETHANOL (UNII: HIE492ZZ3T)
INGR	SODIUM HYDROXIDE (UNII: 55X04QC32I)
INGR	CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		42.5 g in 1 JAR; Type 0: Not a Combination Product
2		85 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
Cosmetic		05/07/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	11/01/2024	05/31/2027

Labeler - DUKE CANNON SUPPLY CO. (078715221)

View All Sections

Published Date (What is this?)	Version	Files
May 9, 2025	2 (current)	download
Nov 8, 2024	1	download

Label: WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

When using this product

Stop use and ask a doctor if

Find additional resources

Safety

Related Resources

More Info on this Drug

Active ingredients	Pupose
Avobenzone 2%	Sunscreen
Octinoxate 6.5%	Sunscreen
Octisalate 5%	Sunscreen
Octocylene 1.5%	Sunscreen

	NDC
1	71782-115-01
2	71782-601-01

Label: WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

When using this product

Stop use and ask a doctor if

Find additional resources

Safety

Related Resources

More Info on this Drug

WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

Number of versions: 2

WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

To receive this label RSS feed

To receive all DailyMed Updates for the last seven days

What will I get with the DailyMed RSS feed?

How to discontinue the RSS feed

Why is DailyMed no longer displaying pill images on the Search Results and Drug Info pages?

WINTER RESCUE KIT- octinoxate, octisalate, octocrylene, avobenzone kit

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.