WELLY SUPERHERO SUPPLIES KIT- alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine hydrochloride, hydrocortisone 
Welly Health PBC

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.

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Welly Superhero Supplies Kit

Instant Hand Sanitizer Gel

Drug Facts

Active ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on skin without soap and water.

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use in eyes, if this happens, rinse thoroughly with water.

Stop use, ask a doctor if, irritation develops and persists for 72 hours.

Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Triple Antibiotic Ointment

Drug Facts

Active Ingredient (in each gram)

Bacitracin zinc 400 units

Neomycin sulfate (3.5mg Neomycin)

Polymyxin B sulfate 5000 units

Purpose

First Aid Antibiotics

Uses

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only

Do not use:

Stop use and ask a doctor if

Keep out of reach of children. If ingested, contact a Poison Control Center right away.

Directions

Inactive Ingredients

petrolatum

Burn Gel

Drug Facts

Active ingredient

Lidocaine HCl 2.0%

Purpose

Topical pain relief

Uses

Temporary pain relief for minor burns

Warnings

External use only

Do not use

Stop use, ask doctor

Keep out of reach of children. If ingested contact a Poison Control Center directly

Directions

Inactive ingredients

aloe vera, carbomer, germaben II, menthol, propylene glycol, purified water, triethanolamine, vitamin E acetate

1% Hydrocortisone Cream

Drug Facts

Active ingredient

Hydrocortisone 1.0%

Purpose

Anti-itch

Uses

Warnings

For external use only

Do not use

Stop use, ask a doctor

Keep out of reach of children. If ingested, contact a Poison Control Center right away

Directions

Inactive ingredients

emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

ASSORTED FIRST AID OINTMENTS

ASSORTED SINGLE USE PACKETS

Distributed by: Welly Health PBC
Minneapolis, MN 55402
1-833-BE-WELLY

Recycle me!

Welly TM www.GetWelly.com

Superhero Supplies

9 - HAND SANITIZER 0.9g (1/32 OZ)

9 - TRIPLE ANTIBIOTIC 0.5g (1/57 OZ)

9 - BURN GEL 0.9G (1/32 OZ)

9 - 1% HYDROCORTISONE 0.9g (1/32 OZ)

Packaging

SuperCmp

SuperKt

WELLY SUPERHERO SUPPLIES KIT 
alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine hydrochloride, hydrocortisone kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72663-140
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72663-140-321 in 1 KIT; Type 0: Not a Combination Product03/01/2019
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 19 POUCH 8.1 mL
Part 29 POUCH 4.5 mL
Part 39 POUCH 8.1 mL
Part 49 POUCH 8.1 mL
Part 1 of 4
ANTISEPTIC 
alcohol gel
Product Information
Item Code (Source)NDC:72663-111
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL666 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
10.9 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/25/2019
Part 2 of 4
ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Item Code (Source)NDC:72663-560
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN6 mg  in 1 mL
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 mL
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B0.77 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
10.5 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B02/25/2019
Part 3 of 4
ANALGESIC 
lidocaine hydrochloride gel
Product Information
Item Code (Source)NDC:72663-500
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
10.9 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/25/2019
Part 4 of 4
ANTI-ITCH 
hydrocortisone cream
Product Information
Item Code (Source)NDC:72663-580
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
WHITE WAX (UNII: 7G1J5DA97F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
10.9 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/25/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/2019
Labeler - Welly Health PBC (116766884)

Revised: 12/2021
Document Id: d4781ec5-7613-9c6f-e053-2995a90a0a22
Set id: d4186754-ed6a-4c59-b841-8f4d7b880cd1
Version: 3
Effective Time: 20211231
 
Welly Health PBC