HUSH ANESTHETIC- lidocaine gel 
HUSH Anesthetic

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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Derma Numb Tattoo Numbing Gel

Active Ingredients

Lidocaine

Purpose

Topical Anesthetic

Warnings

For external use only · Keep out of reach of children

Uses

Before skin is broken apply a thick layer of HUSH Gel in the area to be Tattooed. Spread evenly throughout. Reapply along the edges. Wrap the area with a plastic wrap and allow 1 hour for absorption. Remove the plastic wrap and prep skin for procedure.

Warnings

For external use only · Keep out of the reach of children

Before skin is broken apply a thick layer of HUSH Gel in the area to be Tattooed. Spread evenly throughout. Reapply along the edges. Wrap the area with a plastic wrap and allow 1 hour for absorption. Remove the plastic wrap and prep skin for procedure.

Do Not Use

In Blistered Areas · In the eyes · If allergic to ingredients

Stop Use and ask a doctor if

· skin becomes irritated · condition worsens or symptoms last more than 7 days · symptoms clear up and reoccur within a few days

Inactive ingredients

Water, SD Alchohol 40B, Aloe Barbadensis Leaf Extract, Propylene Glycol, Triethanolamine, Glycerin, Menthol, Chamomile (Chamomilla Recutita) Flower Extract, Calendula Officinalis Flower Extract, Green Tea (Camellia Sinensis) Leaf Extract, Comfrey (Symphytum Officinale) Root Extract, Acrylates/c10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Caprylyl Glycol, Methylisothiazolinone

Other Information

Questions or Comments? Call 305-231-7229 or visit www.HUSHgel.com

Hush 4oz Gel

Hush 2oz Gel

HUSH ANESTHETIC 
lidocaine gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49947-002
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
COMFREY ROOT (UNII: M9VVZ08EKQ)  
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49947-002-04 113.4 g in 1 BOTTLE
2 NDC:49947-002-02 56.7 g in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part348 12/01/2012
Labeler - HUSH Anesthetic (012011309)

Revised: 1/2010
Document Id: 2c28e5a6-6651-4978-92ac-5b24d8daeff0
Set id: 97ae1993-7268-4b7f-92e2-6004337d5650
Version: 2
Effective Time: 20100101
 
HUSH Anesthetic