7-Select After Sun Lidicaine HCl Pain-Relieving Gel with Aloe Vera

7-Select After Sun Lidicaine HCl Pain-Relieving with Aloe Vera by

Drug Labeling and Warnings

7-Select After Sun Lidicaine HCl Pain-Relieving with Aloe Vera by is a Otc medication manufactured, distributed, or labeled by 7-11. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

7-SELECT AFTER SUN LIDICAINE HCL PAIN-RELIEVING WITH ALOE VERA- lidocaine hydrochloride gel 
7-11

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7-Select After Sun Lidicaine HCl Pain-Relieving Gel with Aloe Vera

Active Ingredient

Lidocaine hydrochloride 0.5%

Purpose

External Analgesic

Uses

temporarily relieves pain and itching due to:

• minor skin irritations
• sunburn
• minor burns
• scrapes
• minor cuts
• insect bites

Warnings

• For External Use Only

​Do not use

​in large quantities, particularly over raw surfaces or blistered areas.

When using this product

• avoid contact with eyes. If contact occurs, rinse with water to remove.

Stop use and ask a doctor if

• condition gets worse
• symptoms last more than 7 days
• symptoms clear up and occur again in a few days

Keep out of reach of children.

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

Directions

• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.
• children under 2 years of age: ask a doctor

Inactive Ingredients

aloe barbadensis leaf juice, water, isopropyl alcohol, propylene glycol, glycerin, triethanolamine, carbomer, polysorbate 80, diazolidinyl urea, menthol, disodium EDTA, yellow 5, blue 1

Label

7-Select After Sun Lidicaine HCl Pain-Relieving Gel with Aloe Vera

8 OZ (226 g)

NDC: 10202-950-80

7-SELECT AFTER SUN LIDICAINE HCL PAIN-RELIEVING WITH ALOE VERA 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10202-950
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
WATER (UNII: 059QF0KO0R)
MENTHOL (UNII: L7T10EIP3A)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10202-950-80	226 g in 1 BOTTLE; Type 0: Not a Combination Product	02/21/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/21/2019	05/27/2022

Labeler - 7-11 (007347602)

Revised: 10/2024

Document Id: 2474de35-0c8d-13c4-e063-6394a90ad7ce

34390-5

Set id: baffbbce-d194-6816-e053-2a95a90a49e8

Version: 2

Effective Time: 20241014

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