HALORINNA SUN-SCREEN TRAVEL SPF50- sun screen lotion

HALORINNA SUN-SCREEN TRAVEL SPF50 by

Drug Labeling and Warnings

HALORINNA SUN-SCREEN TRAVEL SPF50 by is a Otc medication manufactured, distributed, or labeled by Guangdong Bisutang Biotechnology Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions
Apply generously and evenly to face and
neck 15-20 minutes before sun exposure.
Reapply at least every 2 hours
Use a water-resistant sunscreen when
swimming or sweating. Sun Protection
Measures. Spending time in the sun increases
your risk of skin cancer and early aging.
To reduce this risk, regularly use a sunscreen
with a Broad Spectrum SPF value of 15 or higher
and other sun protection measures including:
- Limiting time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeved shirts, pants, hats, and sunglasses.
Children under 6 months: Ask a doctor.

INDICATIONS & USAGE

Uses

Helps prevent sunburn

If used as directed with other sun protection

measures (see Directions), decreases the risk

of skin cancer and early aging caused

by the sun.

INACTIVE INGREDIENT

WATER
GLYCERIN
CYCLOPENTASILOXANE
CETEARYL ALCOHOL
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE
PEG-100 STEARATE
GLYCERYL STEARATE
STEARIC ACID
CYCLOHEXASILOXANE
PHENOXYETHANOL
HYDROXYACETOPHENONE
POTASSIUM CETYL PHOSPHATE
SODIUM HYDROXIDE
FRAGRANCE
ALLANTOIN
SILICA
XANTHAN GUM
DIMETHICONE
DISODIUM EDTA
BHT
DIPOTASSIUM PHOSPHATE
SODIUM CARBONATE

WARNINGS

Warnings

Do not use on damaged or broken skin.

For external use only.

When using this product keep out of eyes.

If product gets into the eyes, rinse with water to remove

Stop use and consult a doctor if rash occurs.

ACTIVE INGREDIENT

ETHYLHEXYL METHOXYCINNAMATE-----7.5
OCTOCRYLENE -----3.4937
PHENYLBENZIMIDAZOLE SULFONIC ACID----- 2
BUTYL METHOXYDIBENZOYLMETHANE -----2
CI 77891 -----1.8

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

PURPOSE

Sunscreen

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HALORINNA SUN-SCREEN TRAVEL SPF50 
sun screen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84753-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHENYLBENZIMIDAZOLE SULFONIC ACID (UNII: 9YQ9DI1W42) (PHENYLBENZIMIDAZOLE SULFONIC ACID - UNII:9YQ9DI1W42)	PHENYLBENZIMIDAZOLE SULFONIC ACID	2 g  in 100 mL
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	ETHYLHEXYL METHOXYCINNAMATE	7.5 g  in 100 mL
BUTYL METHOXYDIBENZOYLMETHANE (UNII: G63QQF2NOX) (BUTYL METHOXYDIBENZOYLMETHANE - UNII:G63QQF2NOX)	BUTYL METHOXYDIBENZOYLMETHANE	2 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3.4937 g  in 100 mL
CI 77891 (UNII: 15FIX9V2JP) (CI 77891 - UNII:15FIX9V2JP)	CI 77891	1.8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
XANTHAN GUM (UNII: TTV12P4NEE)
ALLANTOIN (UNII: 344S277G0Z)
SODIUM CARBONATE (UNII: 45P3261C7T)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)
BHT (UNII: 1P9D0Z171K)
GLYCERIN (UNII: PDC6A3C0OX)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CYCLOHEXASILOXANE (UNII: XHK3U310BA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PEG-100 STEARATE (UNII: YD01N1999R)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TRIAMCINOLONE ACETONIDE 21-DIPOTASSIUM PHOSPHATE (UNII: FP1AQ8LL5O)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84753-040-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/23/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/23/2026

Labeler - Guangdong Bisutang Biotechnology Co., LTD (447075429)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Bisutang Biotechnology Co., LTD		447075429	manufacture(84753-040)