GOODSENSE BURN RELIEF GEL- lidocaine hcl gel 
Solskyn Personal Care LLC

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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GoodSense Burn Relief Gel

Active Ingredients

Lidocaine 0.5%

Purpose

Topical Analgesic

Uses

Dosage & Administration

For temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, and poison oak.

Warnings

For external use only

Do not use

Do not use this in large quantities, particularly over raw surfaces or blistered areas.

When using this product

When using this product avoid contact with the eyes.

Stop use and ask a doctor

if condition worsens or if symptoms persist for more than 7 days or symptoms clear up and occur again within a few days.

Keep out of reach of children.

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

Directions

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Blue 5, Carbomer. Disodium, EDTA Glycerin, Menthol, Phenoxyethanol, Polysorbate 20, Propanediol, SD Alcohol (1.85% w/w). Sodium Hydroxide, Water, Yellow 5

Questions or Comments?

www.valuelabels.com

Principal Display Panel

GOODSENSE

BURN RELIEF

GEL

with

Lidocaine HCl

with ALOE

Compare to active ingredients of

Solarcaine

100% satisfaction guaranteed

NET WT 8 OZ (226 g)

PKLA-41212-GSF1

GoodSense Burn Relief Gel Front Label.jpg

GoodSense Burn Relief Gel Back Label.jpg

GOODSENSE BURN RELIEF GEL 
lidocaine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70281-618
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPANEDIOL (UNII: 5965N8W85T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
BASIC YELLOW 5 (UNII: 07BP340B4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70281-618-26226 g in 1 BOTTLE; Type 0: Not a Combination Product01/04/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/04/2019
Labeler - Solskyn Personal Care LLC (080010329)
Establishment
NameAddressID/FEIBusiness Operations
KIK Piedmont LLC078482780manufacture(70281-618)

Revised: 6/2019
Document Id: 8c567735-aabb-6e33-e053-2a95a90abc7a
Set id: 7e9d7986-f372-f3d2-e053-2a91aa0a93a2
Version: 2
Effective Time: 20190628
 
Solskyn Personal Care LLC