Label: GOOD NEIGHBOR PHARMACY ALOE VERA- lidocaine hydrochloride gel
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Contains inactivated NDC Code(s)
NDC Code(s): 24385-083-34 - Packager: Amerisourcebergen Drug Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated July 22, 2015
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- Official Label (Printer Friendly)
- Drug Facts
- Temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts, scrapes
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For external use only
Do not use in large quantities, particularly over raw or blistered areas.
When using this product
• avoid contact with eyes.
Rinse with water if contact occurs.
Stop use and ask a doctor if
• condition worsens
or clear up and occur again within a few days.
• if symptoms persist for more than 7 days.
- Keep out of reach of children.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- Good Neighbor Pharmacy Aloe Vera Gel
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INGREDIENTS AND APPEARANCE
GOOD NEIGHBOR PHARMACY ALOE VERA
lidocaine hydrochloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-083 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 500 g in 100000 mg Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER 940 (UNII: 4Q93RCW27E) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) MENTHOL (UNII: L7T10EIP3A) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24385-083-34 500 mg in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/28/1988 Labeler - Amerisourcebergen Drug Corporation (007914906) Establishment Name Address ID/FEI Business Operations Product Quest Mfg, LLC 927768135 manufacture(24385-083) , label(24385-083)