Label: EQUATE SUNBURN RELIEF WITH ALOE AFTER SUN- lidocaine gel
- NDC Code(s): 49035-788-20
- Packager: Wal-Mart Stores Inc
- 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 January 7, 2022
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- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
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Inactive ingredients
water, aloe barbadensis leaf juice, alcohol denat., propylene glycol, laureth-23, glycerin, polysorbate 20, allantoin, carbomer, triethanolamine, menthyl lactate, disodium EDTA, menthol, aleurites moluccanus seed extract, carica papaya (papaya) fruit extract, colocasia antiquorum root extract, mangifera indica (mango) fruit extract, passiflora incarnata flower extract, plumeria acutifolia flower extract, psidium guajava fruit extract, tocopheryl acetate, tocopherol, phenoxyethanol, benzyl alcohol, fragrance, blue 1.
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INGREDIENTS AND APPEARANCE
EQUATE SUNBURN RELIEF WITH ALOE AFTER SUN
lidocaine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-788 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 8 mg in 1 g Inactive Ingredients Ingredient Name Strength MANGO (UNII: I629I3NR86) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LAURETH-23 (UNII: N72LMW566G) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) ALLANTOIN (UNII: 344S277G0Z) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TROLAMINE (UNII: 9O3K93S3TK) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) EDETATE DISODIUM (UNII: 7FLD91C86K) LEVOMENTHOL (UNII: BZ1R15MTK7) KUKUI NUT OIL (UNII: TP11QR7B8R) PAPAYA (UNII: KU94FIY6JB) COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D) PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z) GUAVA (UNII: 74O70D6VG0) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) PLUMERIA ALBA FLOWER OIL (UNII: T69Z2432CU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-788-20 567 g in 1 BOTTLE; Type 0: Not a Combination Product 11/08/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/08/2017 Labeler - Wal-Mart Stores Inc (051957769)